This report shall not be reproduced, unless in its entirety, without written approval from Kaycha Labs. This report isan Kaycha Labs certification. The results relate only to the material or product analyzed. Test results areconfidential unless explicitly waived otherwise. Void after 1 year from test end date. Cannabinoid content of batchmaterial may vary depending on sampling error. IC=In-control QC parameter, NC=Non-controlled QC parameter,ND=Not Detected, NA=Not Analyzed, ppm=Parts Per Million, ppb=Parts Per Billion. Limit of Detection (LoD) andLimit Of Quantitation (LoQ) are terms used to describe the smallest concentration that can be reliably measured byan analytical procedure. RPD=Reproducibility of two measurements. Action Levels are State determined thresholdsfor human safety for consumption and/or inhalation. The result >99% are variable based on uncertainty ofmeasurement (UM) for the analyte. The UM error is available from the lab upon request.The "Decision Rule" for thepass/fail does not include the UM. The limits are based on F.S. Rule 64-4.310.

Jorge SegredoLab Director

State License # n/aISO Accreditation # 97164 ___________________

Signature

03/31/2020

___________________Signed On

4131 SW 47th AVENUE SUITE 1408

Kaycha Labs1000mg CBD 500mg CBG

N/AMatrix: Derivative

Certificateof Analysis

Sample:DA00304008-001Harvest/Lot ID: 00001

Seed to Sale #00001Batch Date :N/A

Batch#: 00001Sample Size Received: 10 ml

Retail Product Size: 60Ordered : 02/26/20Sampled : 02/26/20

Completed: 03/31/20 Expires: 03/31/21Sampling Method: SOP Client Method

Mar 31, 2020 | Theragreen10800 Hole Ave RiversideCA, 92503

PASSEDPage 1 of 4

PRODUCT IMAGE SAFETY RESULTS MISC.

PesticidesPASSED

Heavy MetalsPASSED

MicrobialsPASSED

MycotoxinsPASSED

ResidualsSolventsPASSED

FilthPASSED

Water ActivityNOT TESTED

MoistureNOT TESTED

TerpenesNOT TESTED

CANNABINOID RESULTS

Total THC

0.000%THC/Container :0.000 mg

Total CBD

2.115%CBD/Container :1218.240 mg

Total Cannabinoids

3.078%Total Cannabinoids/Container:1772.928 mg

CBC CBGA CBG THCV D8-THC CBDV CBN CBDA CBD D9-THC THCA

ND ND 0.963% ND ND ND ND ND 2.115% ND ND

ND ND9.630mg/g ND ND ND ND ND

21.150mg/g ND ND

LOD 0.001 0.001 0.001 0.001 0.001 0.001 0.001 0.001 0.0001 0.0001 0.001

% % % % % % % % % % %

Cannabinoid Profile TestAnalyzed by Weight Extraction date : Extracted By :450 3.1074g 03/11/20 12:03:27 965

Analysis Method -SOP.T.40.020, SOP.T.30.050 Reviewed On - 03/12/20 12:45:57Analytical Batch -DA010869POT Instrument Used : DA-LC-003 CBD Batch Date : 03/11/20 08:47:29

Reagent Dilution Consums. ID

022720.R11 400 180111031020.R04 280653964031020.R03 914C4-914AK

929C6-929HFull spectrum cannabinoid analysis utilizing High Performance Liquid Chromatography with UV detection (HPLC-UV). (Method: SOP.T.30.050 forsample prep and Shimadzu High Sensitivity Method SOP.T.40.020 for analysis. LOQ for all cannabinoids is 1 mg/L).

Label ClaimAnalyte LOD Units ResultCBG/CONTAINER 1 mg 577.800

Filth PASSED

Analyzed By Weight Extraction date LOD(ppm) Extracted By584 1g 03/04/20 584

Analysis Method -SOP.T.40.013 Batch Date : 03/04/20 11:39:28Analytical Batch -DA010687FIL Reviewed On - 03/04/20 12:13:37Instrument Used : Filth/Foreign Material Microscope

This includes but is not limited to hair, insects, feces, packaging contaminants, and manufacturing wasteand by-products. An SH-2B/T Stereo Microscope is use for inspection.

This report shall not be reproduced, unless in its entirety, without written approval from Kaycha Labs. This report isan Kaycha Labs certification. The results relate only to the material or product analyzed. Test results areconfidential unless explicitly waived otherwise. Void after 1 year from test end date. Cannabinoid content of batchmaterial may vary depending on sampling error. IC=In-control QC parameter, NC=Non-controlled QC parameter,ND=Not Detected, NA=Not Analyzed, ppm=Parts Per Million, ppb=Parts Per Billion. Limit of Detection (LoD) andLimit Of Quantitation (LoQ) are terms used to describe the smallest concentration that can be reliably measured byan analytical procedure. RPD=Reproducibility of two measurements. Action Levels are State determined thresholdsfor human safety for consumption and/or inhalation. The result >99% are variable based on uncertainty ofmeasurement (UM) for the analyte. The UM error is available from the lab upon request.The "Decision Rule" for thepass/fail does not include the UM. The limits are based on F.S. Rule 64-4.310.

Jorge SegredoLab Director

State License # n/aISO Accreditation # 97164 ___________________

Signature

03/31/2020

___________________Signed On

4131 SW 47th AVENUE SUITE 1408

Kaycha Labs1000mg CBD 500mg CBG

N/AMatrix : Derivative

Certificate of Analysis PASSEDTheragreen

10800 Hole Ave RiversideCA, 92503Telephone: (951) 768-5292Email: theragreen1@gmail.com

Sample : DA00304008-001Harvest/LOT ID: 00001Batch# : 00001Sampled : 02/26/20Ordered : 02/26/20

Sample Size Received : 10 mlCompleted : 03/31/20Expires: 03/31/21Sample Method : SOP Client Method

Page 2 of 4

Pesticides PASSEDPesticides LOD Units Action Level ResultABAMECTIN B1A 0.01 ppm 0.3 NDACEPHATE 0.01 ppm 3 NDACEQUINOCYL 0.01 ppm 2 NDACETAMIPRID 0.01 ppm 3 NDALDICARB 0.01 ppm 0.1 NDAZOXYSTROBIN 0.01 ppm 3 NDBIFENAZATE 0.01 ppm 3 NDBIFENTHRIN 0.01 ppm 0.5 NDBOSCALID 0.01 PPM 3 NDCAPTAN 0.07 ppm 3 NDCARBARYL 0.05 ppm 0.5 NDCARBOFURAN 0.01 ppm 0.1 NDCHLORANTRANILIPROLE 0.1 ppm 3 NDCHLORFENAPYR 0.01 ppm 0.1 NDCHLORMEQUAT CHLORIDE 0.05 ppm 3 NDCHLORPYRIFOS 0.01 ppm 0.1 NDCLOFENTEZINE 0.02 ppm 0.5 NDCOUMAPHOS 0.01 ppm 0.1 NDCYFLUTHRIN 0.05 ppm 1 NDCYPERMETHRIN 0.05 ppm 1 NDDAMINOZIDE 0.01 ppm 0.1 NDDIAZANON 0.01 ppm 0.2 NDDICHLORVOS 0.01 ppm 0.1 NDDIMETHOATE 0.01 ppm 0.1 NDDIMETHOMORPH 0.02 ppm 3 NDETHOPROPHOS 0.01 ppm 0.1 NDETOFENPROX 0.01 ppm 0.1 NDETOXAZOLE 0.01 ppm 1.5 NDFENHEXAMID 0.01 ppm 3 NDFENOXYCARB 0.01 ppm 0.1 NDFENPYROXIMATE 0.01 ppm 2 NDFIPRONIL 0.01 ppm 0.1 NDFLONICAMID 0.01 ppm 2 NDFLUDIOXONIL 0.01 ppm 3 NDHEXYTHIAZOX 0.01 ppm 2 NDIMAZALIL 0.01 ppm 0.1 NDIMIDACLOPRID 0.04 ppm 3 NDKRESOXIM-METHYL 0.01 ppm 1 NDMALATHION 0.02 ppm 2 NDMETALAXYL 0.01 ppm 3 NDMETHIOCARB 0.01 ppm 0.1 ND

Pesticides LOD Units Action Level ResultMETHOMYL 0.01 ppm 0.1 NDMETHYL PARATHION 0.005 ppm 0.1 NDMEVINPHOS 0.01 ppm 0.1 NDMYCLOBUTANIL 0.01 ppm 3 NDNALED 0.025 ppm 0.5 NDOXAMYL 0.05 ppm 0.5 NDPACLOBUTRAZOL 0.01 ppm 0.1 NDPHOSMET 0.01 ppm 0.2 NDPIPERONYL BUTOXIDE 0.1 ppm 3 NDPRALLETHRIN 0.01 ppm 0.4 NDPROPICONAZOLE 0.01 ppm 1 NDPROPOXUR 0.01 ppm 0.1 NDPYRETHRINS 0.05 ppm 1 NDPYRIDABEN 0.02 ppm 3 NDSPINETORAM 0.02 PPM 3 NDSPIROMESIFEN 0.01 ppm 3 NDSPIROTETRAMAT 0.01 ppm 3 NDSPIROXAMINE 0.01 ppm 0.1 NDTEBUCONAZOLE 0.01 ppm 1 NDTHIACLOPRID 0.01 ppm 0.1 NDTHIAMETHOXAM 0.05 ppm 1 NDTOTAL CONTAMINANT LOAD(PESTICIDES)

0 ppm 20 ND

TOTAL PERMETHRIN 0.01 ppm 1 NDTOTAL SPINOSAD 0.01 ppm 3 NDTRIFLOXYSTROBIN 0.01 ppm 3 NDCHLORDANE * 0.01 ppm 0.1 NDPCNB * 0.01 ppm 0.2 ND

Pesticides PASSED

Analyzed by Weight Extraction date Extracted By585 , 1.0223g 03/04/20 12:03:08 1082 , 584

Analysis Method - SOP.T.30.065, SOP.T.40.065,SOP.T40.060, SOP.T.40.070 and SOP.T.40.090 ,SOP.T.30.065, SOP.T.40.065, SOP.T40.060 andSOP.T.40.090Analytical Batch - DA010680PES , DA010690 Reviewed On- 03/04/20 12:13:37Instrument Used : DA-LCMS-001_DERBatch Date : 03/04/20 09:34:44

Reagent Dilution Consums. ID013120.30 10 180111022720.R13 280653964030420.R04

Pesticide screen is performed using LC-MS which can screen down to below single digit ppb concentrationsfor regulated Pesticides. Currently we analyze for 67 Pesticides. (Method: SOP.T.30.060 Sample Preparationfor Pesticides Analysis via LCMSMS and SOP.T40.060 Procedure for Pesticide Quantification Using LCMS).Volatile Pesticides may be tested with GCMSMS under SOP.T.40.070 and SOP.T.40.090. * Pesticide screen isperformed using GC-MS which can screen down to below single digit ppb concentrations for regulatedPesticides. Currently we analyze for 2 Volatile Pesticides. (Method: SOP.T.30.060 Sample Preparation forPesticides Analysis via LCMSMS and SOP.T.40.090 Volatile Pesticides Analysis by GC-MS/MS

This report shall not be reproduced, unless in its entirety, without written approval from Kaycha Labs. This report isan Kaycha Labs certification. The results relate only to the material or product analyzed. Test results areconfidential unless explicitly waived otherwise. Void after 1 year from test end date. Cannabinoid content of batchmaterial may vary depending on sampling error. IC=In-control QC parameter, NC=Non-controlled QC parameter,ND=Not Detected, NA=Not Analyzed, ppm=Parts Per Million, ppb=Parts Per Billion. Limit of Detection (LoD) andLimit Of Quantitation (LoQ) are terms used to describe the smallest concentration that can be reliably measured byan analytical procedure. RPD=Reproducibility of two measurements. Action Levels are State determined thresholdsfor human safety for consumption and/or inhalation. The result >99% are variable based on uncertainty ofmeasurement (UM) for the analyte. The UM error is available from the lab upon request.The "Decision Rule" for thepass/fail does not include the UM. The limits are based on F.S. Rule 64-4.310.

Jorge SegredoLab Director

State License # n/aISO Accreditation # 97164 ___________________

Signature

03/31/2020

___________________Signed On

4131 SW 47th AVENUE SUITE 1408

Kaycha Labs1000mg CBD 500mg CBG

N/AMatrix : Derivative

Certificate of Analysis PASSEDTheragreen

10800 Hole Ave RiversideCA, 92503Telephone: (951) 768-5292Email: theragreen1@gmail.com

Sample : DA00304008-001Harvest/LOT ID: 00001Batch# : 00001Sampled : 02/26/20Ordered : 02/26/20

Sample Size Received : 10 mlCompleted : 03/31/20Expires: 03/31/21Sample Method : SOP Client Method

Page 3 of 4

Residual Solvents PASSED

Solvent LOD Units ActionLevel(PPM)

Pass/Fail Result

1,1-DICHLOROETHENE 1 ppm 8 PASS ND

1,2-DICHLOROETHANE 0.18 ppm 2 PASS ND

2-PROPANOL 45 ppm 500 PASS ND

ACETONE 67.5 ppm 750 PASS ND

ACETONITRILE 5.4 ppm 60 PASS ND

BENZENE 0.09 ppm 1 PASS ND

BUTANES (N-BUTANE) 96 ppm 5000 PASS ND

CHLOROFORM 0.18 ppm 2 PASS ND

DICHLOROMETHANE 3.75 ppm 125 PASS ND

ETHANOL 90 ppm PASS ND

ETHYL ACETATE 36 ppm 400 PASS ND

ETHYL ETHER 45 ppm 500 PASS ND

ETHYLENE OXIDE 0.6 ppm 5 PASS ND

HEPTANE 45 ppm 5000 PASS ND

METHANOL 22.5 ppm 250 PASS ND

N-HEXANE 4.5 ppm 250 PASS ND

PENTANES (N-PENTANE) 67.5 ppm 750 PASS ND

PROPANE 120 ppm 5000 PASS ND

TOLUENE 13.5 ppm 150 PASS ND

TOTAL XYLENES 13.5 ppm 150 PASS ND

TRICHLOROETHYLENE 2.25 ppm 25 PASS ND

Residual Solvents PASSED

Analyzed by Weight Extraction date Extracted By850 0.0209g 03/04/20 02:03:36 850

Analysis Method -SOP.T.40.032Analytical Batch -DA010661SOL Reviewed On - 03/05/20 12:14:42Instrument Used : Headspace GCMSBatch Date : 03/03/20 15:49:14

Reagent Dilution Consums. ID

1 00279984161291-124154107

Residual solvents screening is performed using GC-MS which can detect belowsingle digit ppm concentrations. Currently we analyze for 21 Residualsolvents.(Method: SOP.T.30.032 Residual Solvents Analysis via GC-MS).

This report shall not be reproduced, unless in its entirety, without written approval from Kaycha Labs. This report isan Kaycha Labs certification. The results relate only to the material or product analyzed. Test results areconfidential unless explicitly waived otherwise. Void after 1 year from test end date. Cannabinoid content of batchmaterial may vary depending on sampling error. IC=In-control QC parameter, NC=Non-controlled QC parameter,ND=Not Detected, NA=Not Analyzed, ppm=Parts Per Million, ppb=Parts Per Billion. Limit of Detection (LoD) andLimit Of Quantitation (LoQ) are terms used to describe the smallest concentration that can be reliably measured byan analytical procedure. RPD=Reproducibility of two measurements. Action Levels are State determined thresholdsfor human safety for consumption and/or inhalation. The result >99% are variable based on uncertainty ofmeasurement (UM) for the analyte. The UM error is available from the lab upon request.The "Decision Rule" for thepass/fail does not include the UM. The limits are based on F.S. Rule 64-4.310.

Jorge SegredoLab Director

State License # n/aISO Accreditation # 97164 ___________________

Signature

03/31/2020

___________________Signed On

4131 SW 47th AVENUE SUITE 1408

Kaycha Labs1000mg CBD 500mg CBG

N/AMatrix : Derivative

Certificate of Analysis PASSEDTheragreen

10800 Hole Ave RiversideCA, 92503Telephone: (951) 768-5292Email: theragreen1@gmail.com

Sample : DA00304008-001Harvest/LOT ID: 00001Batch# : 00001Sampled : 02/26/20Ordered : 02/26/20

Sample Size Received : 10 mlCompleted : 03/31/20Expires: 03/31/21Sample Method : SOP Client Method

Page 4 of 4

Mycotoxins PASSED

Analyte LOD Units Result Action Level (PPM)AFLATOXIN G2 0.002 ppm ND 0.02AFLATOXIN G1 0.002 ppm ND 0.02AFLATOXIN B2 0.002 ppm ND 0.02AFLATOXIN B1 0.002 ppm ND 0.02OCHRATOXIN A+ 0.002 ppm ND 0.02

Analysis Method -SOP.T.30.065, SOP.T.40.065Analytical Batch -DA010681 | Reviewed On - 03/05/20 14:20:10Instrument Used : DA-LCMS-001_DERBatch Date : 03/04/20 09:35:57

Analyzed by Weight Extraction date Extracted By585 1g 03/04/20 01:03:39 585

Aflatoxins B1, B2, G1, G2, and Ochratoxins A testing using LC-MS. (Method: SOP.T.30.065 forSample Preparation and SOP.T40.065 Procedure for Mycotoxins Quantification Using LCMS. LOQ 1.0ppb). Aflatoxin B1, B2, G1, and G2 must individually be <20ug/Kg. Ochratoxins must be <20µg/Kg.

Microbials PASSED

Analyte ResultASPERGILLUS_FLAVUS not present in 1 gram.ASPERGILLUS_FUMIGATUS not present in 1 gram.ASPERGILLUS_NIGER not present in 1 gram.ASPERGILLUS_TERREUS not present in 1 gram.ESCHERICHIA_COLI_SHIGELLA_SPP not present in 1 gram.SALMONELLA_SPECIFIC_GENE not present in 1 gram.

Analysis Method -SOP.T.40.043Analytical Batch -DA010675MIC | Reviewed On - 03/05/20 15:57:35Instrument Used : PathogenDX PCR_Array Scanner,PathogenDX PCR_DA-010Batch Date : 03/04/20 09:11:21

Analyzed by Weight Extraction date Extracted By513 1.0430g 03/04/20 10:03:28 1082

Reagent Dilution Consums. ID

082019.46 181019-274

121619.09 SG298A

Reagent Consums. ID013120.327013120.258013120.400122719.50020320.68013120.338020420.381013120.399121719.06121719.12

918C4-918J914C4-914AK929C6-929H50AX262191906116341932323819111

Microbiological testing for Fungal and Bacterial Identification via Polymerase Chain Reaction (PCR)method consisting of sample DNA amplified via tandem Polymerase Chain Reaction (PCR) as acrude lysate which avoids purification. (Method SOP.T.40.043) If a pathogenic Escherichia Coli,Salmonella, Aspergillus fumigatus, Aspergillus flavus, Aspergillus niger, or Aspergillus terreus isdetected in 1g of a sample, the sample fails the microbiological-impurity testing.

Heavy Metals PASSED

Reagent Reagent Dilution030320.R13030420.R05030220.R01030220.R02030420.R03030420.R02

030420.R01030320.R12111319.02

50

Metal LOD Unit Result Action Level (PPM)

ARSENIC 0.02 ppm ND 1.5CADMIUM 0.02 ppm ND 0.5LEAD 0.02 ppm ND 0.5MERCURY 0.02 ppm ND 3

Analyzed by Weight Extraction date Extracted By53 0.2597g 03/04/20 11:03:04 457

Analysis Method -SOP.T.40.050, SOP.T.30.052Analytical Batch -DA010672HEA | Reviewed On - 03/05/20 07:39:58Instrument Used : ICPMS-2030Batch Date : 03/04/20 08:54:39

Heavy Metals screening is performed using ICP-MS (Inductively Coupled Plasma – MassSpectrometer) which can screen down to below single digit ppb concentrations for regulated heavymetals using Method SOP.T.30.052 Sample Preparation for Heavy Metals Analysis via ICP-MS andSOP.T.40.050 Heavy Metals Analysis via ICP-MS.