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.

Anthony SmithLab Director

State License #010-10166277B9D

ISO Accreditation # 99861___________________Signature

07/13/21

___________________Signed On

540 E Vilas Rd Suite FCentral Point, OR, 97502, US

Kaycha LabsStress Caps STR-21701D

N/ASample Type: Ingestible

Certificateof Analysis

Sample:CE10708005-001Harvest/Lot ID: 6510IHH-STR2101

Metrc #: N/AMetrc Source Package #: N/A

Batch Date: 06/23/21Batch#: STR-21701D

Sample Size Received: 8.29 gramTotal Weight/Volume: 16414 gram gram

Retail Product Size: 0.4 gramOrdered : 07/08/21sampled : 07/08/21

Completed: 07/13/21 Expires: 07/13/22Sampling Method: SOP-024

Jul 13, 2021 | Indomira/Green EarthMedicinalsLicense #8147 Blackwell RdCentral Point, OR, 97502, US

Page 1 of 2

PRODUCT IMAGE SAFETY RESULTS MISC.

PesticidesNOT TESTED

Heavy MetalsNOT TESTED

MicrobialsNOT TESTED

MycotoxinsNOT TESTED

ResidualsSolvents

NOT TESTED

FilthNOT TESTED

Water ActivityNOT TESTED

MoistureNOT TESTED

HomogeneityNOT TESTED

TerpenesNOT

TESTEDCANNABINOID RESULTS

Total THC

0.070%Total CBD

2.392%Total Cannabinoids

2.652%

CBDV CBDVA CBG CBD CBDA THCV CBGA CBN D9-THC D8-THC THCVA CBC THCA CBCA% <LOQ <LOQ 0.0245 2.3131 0.0902 <LOQ <LOQ <LOQ 0.0707 <LOQ <LOQ 0.1543 <LOQ <LOQmg/g <LOQ <LOQ 0.25 23.13 0.90 <LOQ <LOQ <LOQ 0.71 <LOQ <LOQ 1.54 <LOQ <LOQLOQ 0.002 0.002 0.002 0.002 0.002 0.002 0.002 0.002 0.002 0.002 0.002 0.002 0.002 0.002

% % % % % % % % % % % % % %

Cannabinoid Profile TestAnalyzed by Weight Extraction date : Extracted By :11 1.015g 07/09/21 02:07:07 13

Analysis Method -SOP.T.40.020, SOP.T.30.050 Reviewed On - 07/13/21 15:14:58 Batch Date : 07/09/21 14:16:46Analytical Batch -CE000147POT Instrument Used : HPLC 2030 EID 005 - Low

ConcentrationRunning On :

Reagent Dilution Consums. ID Consums. ID062821.R09062221.01

40 D0149306932009E-1232436020160AS3 436020338AS2 436021005AS3C0000642041CD-041C042C4-042AL

F1485600325891

"Total THC" and "Total CBD" are calculated values and are an Oregon reporting requirement (OAR 333-064-0100). For Cannabinoid analysis, only delta 9-THC, THCA, CBD, CBDA are ORELAP accreditedanalytes. Cannabinoid values reported for plant matter are dry weight corrected; Instrument LOQ for all cannabinoids is 0.5 mg/mL, LOQ 'in matrix' is dependent on extraction parameters. FD = FieldDuplicate; LOQ = Limit of Quantitation.

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.

Anthony SmithLab Director

State License #010-10166277B9D

ISO Accreditation # 99861___________________Signature

07/13/21

___________________Signed On

540 E Vilas Rd Suite FCentral Point, OR, 97502, US

Kaycha LabsStress Caps STR-21701D

N/ASample Type : Ingestible

POTENCY BATCH QC REPORTPage 2 of 2

METHOD BLANK

Cannabinoid LOQ Result UnitsCBDV_WET 0.002 <LOQ %CBDVA_WET 0.002 <LOQ %THCV_WET 0.002 <LOQ %CBD_WET 0.002 <LOQ %CBG_WET 0.002 <LOQ %CBDA_WET 0.002 <LOQ %CBN_WET 0.002 <LOQ %CBGA_WET 0.002 <LOQ %THCVA_WET 0.002 <LOQ %D9-THC_WET 0.002 <LOQ %D8-THC_WET 0.002 <LOQ %CBC_WET 0.002 <LOQ %THCA_WET 0.002 <LOQ %CBC-A_WET 0.002 <LOQ %TOTAL CANNABINOIDS 0.002 <LOQ %TOTAL CBD 0.002 <LOQ %TOTAL THC 0.002 <LOQ %CBDV 0.002 <LOQ %CBDVA 0.002 <LOQ %CBG 0.002 <LOQ %CBD 0.002 <LOQ %CBDA 0.002 <LOQ %THCV 0.002 <LOQ %CBGA 0.002 <LOQ %CBN 0.002 <LOQ %D9-THC 0.002 <LOQ %D8-THC 0.002 <LOQ %THCVA 0.002 <LOQ %CBC 0.002 <LOQ %THCA 0.002 <LOQ %CBCA 0.002 <LOQ %

Analytical Batch - CE000147POTInstrument Used : HPLC 2030 EID 005 - Low Concentration

LCS

Cannabinoid LOQ Recovery Units Recovery LimitsCBG_WET 0.002 84.5 % 70-130CBD_WET 0.002 85.4 % 70-130CBDA_WET 0.002 84.3 % 70-130THCV_WET 0.002 92.8 % 70-130CBGA_WET 0.002 82.5 % 70-130CBN_WET 0.002 89.3 % 70-130D9-THC_WET 0.002 87.6 % 70-130CBC_WET 0.002 84.0 % 70-130THCA_WET 0.002 81.9 % 70-130CBC-A_WET 0.002 77.1 % 70-130

Analytical Batch - CE000147POTInstrument Used : HPLC 2030 EID 005 - Low Concentration

Cannabinoid Potency Batch Quality Report: OLCC/ODA Control Study ID: unk.

Sample Lab IDTotal THC

(mg/g)Total CBD

(mg/g)THCA

(mg/g)Δ9-THC (mg/g)

CBD-A (mg/g)

CBD (mg/g)

Stress Caps STR 21701D CE10708005-001 0.70 23.92 <LOQ 0.71 0.90 23.13

Stress Caps STR 21701D FD

CE10708005-002 0.70 23.90 <LOQ 0.71 0.09 23.09

Average 0.70 23.91 #DIV/0! 0.71 0.50 23.11

RPD 0.00% 0.08%

RPD Status: PASS

540 E. Vilas Rd., Suite FCentral Point, OR 97502www.kaychalabs.com Anthony Smith, Ph.D

541.668.7444This report shall not be reproduced, unless in its entirety, without written approval from Kaycha Labs and KGO, LLC. This report is a Kaycha Labs certification. The results relate only to the material or product analyzed. Test results are confidential unless explicitly waived otherwise. Void after 1 year from test end date. Cannabinoid content of batch material may vary depending on sampling error. Sampling method: KR-SOP-018; ORELAP-SOP-002.

KGO-BQR-CE10708005-001_002 Indomira-GEM

KML Laboratories, Inc.

261 Great Northern Road Bonners Ferry, Idaho 83805 Phone: 208-267-0818 Fax: 208-267-0878 Email: Info@kmlmicro.com

Certificate of Analysis Green Earth Medicinals Invoice Number: 21.0902 2305 Ashland St, Suite C360 PO Number: 071221 Ashland, OR 97520 Received Date: 07/14/2021 Phone: 888-620-1110 Number of Samples: 01 Fax: Project Name: Routine Testing

Confidential Page 1 of 2 This Certificate/Report shall not be reproduced, except in full, without the prior written consent of KML Laboratories, Inc. This report may include work not covered by KML’s current ISO accreditation as indicated by ‡. Note: On this date, this material met the specifications designated above, and is not known if statistically representative of the lot evaluated on a routine basis. This information is not intended to relieve the purchaser from its responsibility to determine the suitability of this material for purchaser’s purposes, to comply with all laws and regulations regarding the safe use of this material. nd = none detected above the listed detection limit F10-0817 G Ref SOP 01-023

_______ AT-1805

Microbiology Report: Lab #: 21-7180 Sample Lot: STR-21701D Sample Date: 07/08/2021 Sample Name: CBD+ Stress Support Caps Additional ID: Plated Date: 07/14/2021 Qualifying Material Number: No QM

Test Performed Results Units Detection Limit Method Date Analyzed

Aerobic Plate Count 15 cfu/g 10 USP 43-NF 38 <2021> 07/17/2021 Coliforms nd cfu/g 10 Bam C4 sec G 07/15/2021 E. coli absent P/A 1 USP 43-NF 38 <2022> 07/17/2021 Staph aureus absent P/A 1 USP 43-NF 38 <2022> 07/17/2021 Yeast nd cfu/g 10 USP 43-NF 38 <2021> 07/19/2021 Mold nd cfu/g 10 USP 43-NF 38 <2021> 07/19/2021 Salmonella absent P/A 1 USP 43-NF 38 <2022> 07/18/2021 Pseudo. aeruginosa absent P/A 1 USP 43-NF 38 <m62> 07/17/2021

Approved By: QA Director SMV 07/19/2021

KML Laboratories, Inc.

261 Great Northern Road Bonners Ferry, Idaho 83805 Phone: 208-267-0818 Fax: 208-267-0878 Email: Info@kmlmicro.com

Certificate of Analysis Green Earth Medicinals Invoice Number: 21.0902 2305 Ashland St, Suite C360 PO Number: 071221 Ashland, OR 97520 Received Date: 07/14/2021 Phone: 888-620-1110 Number of Samples: 01 Fax: Project Name: Routine Testing

Confidential Page 2 of 2 This Certificate/Report shall not be reproduced, except in full, without the prior written consent of KML Laboratories, Inc. This report may include work not covered by KML’s current ISO accreditation as indicated by ‡. Note: On this date, this material met the specifications designated above, and is not known if statistically representative of the lot evaluated on a routine basis. This information is not intended to relieve the purchaser from its responsibility to determine the suitability of this material for purchaser’s purposes, to comply with all laws and regulations regarding the safe use of this material. nd = none detected above the listed detection limit F10-0817 G Ref SOP 01-023

_______ AT-1805

Microbiology Report: Lab #: Control 07142021 Additional ID: Negative Control Purposes Plated Date: 07/14/2021 Sample Name: Control 07142021 Qualifying Material Number: QM-06-001

Test Performed Results Units Detection Limit Method Date Analyzed

Aerobic Plate Count nd cfu/ml 10 USP 43-NF 38 <2021> 07/17/2021 Coliforms nd cfu/ml 10 Bam C4 sec G 07/15/2021 E. coli absent P/A 1 USP 43-NF 38 <2022> 07/17/2021 Staph aureus absent P/A 1 USP 43-NF 38 <2022> 07/17/2021 Yeast nd cfu/ml 10 USP 43-NF 38 <2021> 07/19/2021 Mold nd cfu/ml 10 USP 43-NF 38 <2021> 07/19/2021 Salmonella absent P/A 1 USP 43-NF 38 <2022> 07/18/2021 Pseudo. aeruginosa absent P/A 1 USP 43-NF 38 <m62> 07/17/2021

Approved By: QA Director SMV 07/19/2021