This report shall not be reproduced, unless in its entirety, without written approval from Kaycha Labs. This report is an 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. 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) and Limit Of Quantitation (LoQ) are terms used to describe the smallest concentration that can be reliably measured by an analytical procedure. RPD=Reproducibility of two measurements. Action Levels are State determined thresholds for human safety for consumption and/or inhalation. The result >99% are variable based on uncertainty of measurement (UM) for the analyte. The UM error is available from the lab upon request.The "Decision Rule" for the pass/fail does not include the UM. The limits are based on F.S. Rule 64-4.310. Anthony Smith Lab Director State License # 010-10166277B9D ISO Accreditation # 99861 ___________________ Signature 07/13/21 ___________________ Signed On 540 E Vilas Rd Suite F Central Point, OR, 97502, US Kaycha Labs Stress Caps STR-21701D N/A Sample Type: Ingestible Certificate of Analysis Sample:CE10708005-001 Harvest/Lot ID: 6510IHH-STR2101 Metrc #: N/A Metrc Source Package #: N/A Batch Date: 06/23/21 Batch#: STR-21701D Sample Size Received: 8.29 gram Total Weight/Volume: 16414 gram gram Retail Product Size: 0.4 gram Ordered : 07/08/21 sampled : 07/08/21 Completed: 07/13/21 Expires: 07/13/22 Sampling Method: SOP-024 Jul 13, 2021 | Indomira/Green Earth Medicinals License # 8147 Blackwell Rd Central Point, OR, 97502, US Page 1 of 2 PRODUCT IMAGE SAFETY RESULTS MISC. Pesticides NOT TESTED Heavy Metals NOT TESTED Microbials NOT TESTED Mycotoxins NOT TESTED Residuals Solvents NOT TESTED Filth NOT TESTED Water Activity NOT TESTED Moisture NOT TESTED Homogeneity NOT TESTED Terpenes NOT TESTED CANNABINOID 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 <LOQ mg/g <LOQ <LOQ 0.25 23.13 0.90 <LOQ <LOQ <LOQ 0.71 <LOQ <LOQ 1.54 <LOQ <LOQ LOQ 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 Test Analyzed 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 14:16:46 Analytical Batch -CE000147POT Instrument Used : HPLC 2030 EID 005 - Low Concentration Running On : Reagent Dilution Consums. ID Consums. ID 062821.R09 062221.01 40 D01493069 32009E-1232 436020160AS3 436020338AS2 436021005AS3 C0000642 041CD-041C 042C4-042AL F148560 0325891 "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 accredited analytes. 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 = Field Duplicate; LOQ = Limit of Quantitation.
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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
"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
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.
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
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