Transparency Report

Product Quality & Formula Verification

A customer-facing summary of the formula, manufacturer Certificate of Analysis (COA), ingredient verification, contaminant testing, and manufacturing quality information for The Change Within™.

11 Active IngredientsHeavy Metals: PassMicrobiology: PassU.S. ManufacturedNSF/ANSI 455-2SQF Certified
Transparency Note
This report summarizes manufacturer and formula documentation for the underlying Women's Vitality / Women's Support capsule formula. The COA referenced below is batch-specific. Future production lots should be matched to their own lot-specific COA before making batch-specific claims.

At a Glance

11 ACTIVE INGREDIENTS
Every active ingredient listed on the formula is accounted for in the referenced manufacturer COA.
HEAVY METALS: PASS
Lead and arsenic were below stated limits; cadmium and mercury were not detected for the referenced lot.
MICROBIOLOGY: PASS
E. coli, Salmonella and Staphylococcus aureus were negative; plate count and yeast/mold were well below limits.
U.S. MANUFACTURED
COA identifies the manufacturing facility as Vitalabs, Inc. in McDonough, Georgia, USA.
NSF/ANSI 455-2
COA lists facility certification number C0199998-HSCDS-5.
SQF CERTIFIED
COA lists GFSI SQF certification number 72660.

Referenced COA

Manufacturer documentCertificate of Analysis – Women's Support Capsules
ManufacturerVitalabs, Inc. (McDonough, Georgia, USA)
Product codeVLI210-04
Customer master batch lot70927
Manufacturer lot244037
Manufactured03/2025
Expiration04/2027
COA approval date01/21/2026
Serving size2 capsules
Important: "FDA-registered facility" is not the same as "FDA approved." Dietary supplements are not FDA-approved products. The formula is also listed as Non-GMO in current product documentation; the COA itself does not present a separate Non-GMO certification.

Full Ingredient Profile & COA Verification

Serving size: 2 capsules | 60 capsules per bottle (30 servings). The table below reproduces the label-claim amount and the result reported on the referenced manufacturer COA.

Active IngredientLabel ClaimCOA Result% ClaimMethod
Red Clover Aerial Parts Extract (1%)400 mg400.00 mg100.00%ID-HPLC
Sage Leaf Extract (2.5%)200 mg262.40 mg131.20%HPLC
Black Cohosh Root Extract160 mg160.00 mg100.00%ID by UV
Dong Quai Root Extract (1%)150 mg150.00 mg100.00%ID-HPLC
Licorice Root Extract (1%)150 mg150.00 mg100.00%ID-HPLC
Chasteberry Fruit Extract (0.5%)50 mg50.00 mg100.00%ID by HPLC
Blessed Thistle Herb Powder50 mg50.00 mg100.00%ID by FTIR
Red Raspberry Fruit Powder50 mg50.00 mg100.00%ID by HPTLC
Soy Isoflavones30 mg35.43 mg118.10%HPLC
Wild Yam Root Extract (16%)15 mg18.87 mg125.83%HPLC
trans-Resveratrol (from Polygonum cuspidatum root)1 mg1.34 mg134.00%HPLC

How to read this table: HPLC rows are quantitative assays. Several botanicals are identified in the COA through validated identity methods (UV, HPLC identity, FTIR, or HPTLC) and are reported at the label-claim amount. The manufacturer COA notes that certain finished-product specifications may be verified through raw-material identification, process controls, and QA batch-record review under 21 CFR 111.75(d)(1), rather than direct finished-batch quantification.

Other Ingredients

Gelatin (bovine), Microcrystalline Cellulose, Vegetable Magnesium Stearate, Silicon Dioxide.

Allergen & Dietary Information

ContainsSoy
Bovine-derived capsuleYes – gelatin (bovine)
Vegetarian / veganNo
Facility cross-contact noticeCurrent formula documentation states the product is manufactured/packaged in a facility that may also process milk, soy, wheat, egg, peanuts, tree nuts, fish and crustacean shellfish.

Safety, Purity & Microbiology Results

The referenced COA reports the following contaminant and microbiological results for the lot shown in this document.

Heavy MetalSpecificationCOA ResultStatus
Lead≤ 2.75 mcg per serving0.393 mcg / 2 capsulesPASS
Arsenic≤ 10 mcg per serving0.054 mcg / 2 capsulesPASS
Cadmium≤ 4.1 mcg per servingNot DetectedPASS
Mercury≤ 3 mcg per servingNot DetectedPASS
Microbial TestSpecificationCOA ResultStatus
Standard Plate Count< 10,000 cfu/g< 10 cfu/gPASS
Yeast & Mold< 1,000 cfu/g< 10 cfu/gPASS
E. coliNegative / 10 gNegativePASS
SalmonellaNegative / 10 gNegativePASS
Staphylococcus aureusNegative / 10 gNegativePASS

Manufacturing Quality Documentation

NSF/ANSI 455-2Certification number C0199998-HSCDS-5 is printed on the referenced COA.
SQF / GFSICertification number 72660 is printed on the referenced COA.
Country / facilityVitalabs, Inc. — McDonough, Georgia, USA (per referenced COA).
FDA registration statusUpstream compliance documentation states the manufacturing facilities used for this catalog are FDA-registered. FDA registration is not FDA approval.
Non-GMO designationCurrent formula documentation identifies the formula as Non-GMO. This report does not represent a separate third-party Non-GMO certification.

View the Source Documents

Every figure on this page is drawn from the manufacturer's own Certificate of Analysis. You're welcome to review the full document yourself below.

Consumer Safety Note
Do not exceed the recommended dose. Consult a healthcare professional before use if pregnant or nursing, under 18, taking medication, using hormone therapy, or managing a medical or hormone-sensitive condition. Keep out of reach of children. Do not use if the safety seal is damaged or missing. Store in a cool, dry place.

*These statements have not been evaluated by the Food and Drug Administration. This product is not intended to diagnose, treat, cure, or prevent any disease. This document is a transparency summary of available product and manufacturer documentation and is not a substitute for medical advice or the lot-specific original COA.