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iSatori

Isa-Test GF

Serving
4 Capsule(s)
Per container
30
Form
capsule-unknown
UPC
883488005077
DSLD
217093
Formula hash
ee41db95a299
Brand context
iSatori
CA
Catalog
74
products
With avoid flag
9
products
FDA recalls
0
history
CAERS
1
reports
Caution-flaggedObjective label signals
Flagged excipients
3
0 avoid · 3 caution
FDA recalls
0
no recall history
CAERS reports
1
FDA consumer events
Certifications
0
none recorded
3 excipients carry authority-caution citations. · Every flag below links to the authority's published citation.

Supplement Facts

7 active ingredients
IngredientAmount% DV
Vitamin C
vitaminUNII · PQ6CK8PD0R
UL · set5 effects
25 mg28%
Vitamin B6
vitaminUNII · KV2JZ1BI6Z
UL · set6 effects
7 mg412%
Magnesium
mineralUNII · I38ZP9992A
UL · set6 effects
300 mg71%
Zinc
mineralUNII · J41CSQ7QDS
UL · set8 effects
20 mg182%
ISA-Test GF
Proprietary Blend (Herb/Botanical)other
1714 mg—
Somatrin
Proprietary Blend (Combination)other
325 mg—
Isaflow
Proprietary Blend (Herb/Botanical)other
100 mg—
What this product supports · authorized claims

17 authority-backed effects

Rolled up from EFSA / FDA / NIH ODS authorized function claims on this product's active ingredients. Each row shows which ingredients contribute.

Flagged excipients

3 flagged · authority citations

  • ◐ CAUTIONFD&C Red #40
    color

    EU requires the same 'attention/activity in children' warning label as Yellow 5 per Commission Regulation 1333/2008 Annex III. California enacted a public-school ban effective 2028 (AB 2316, 2024).

    eur-lex.europa.eu →leginfo.legislature.ca.gov →
  • ◐ CAUTIONFD&C Red #3
    color

    FDA revoked food/ingested-drug color additive approval for FD&C Red 3 in January 2025 (Docket FDA-2022-C-2886). Manufacturers have until January 2027 (foods) / January 2028 (ingested drugs) to reformulate.

    fda.gov →federalregister.gov →
  • ◐ CAUTIONFD&C Blue #1
    color

    EU requires 'attention in children' warning per Commission Regulation 1333/2008 Annex III. Limited to specific food categories; capsule-shell use permitted with restrictions.

    eur-lex.europa.eu →
FDA CAERS · adverse event context
1
consumer-submitted adverse event reports filed with the FDA CFSAN Adverse Event Reporting System mentioning this product or its brand.

CAERS reports are unverified consumer submissions — not adjudicated causality. Large well-known brands accumulate proportionally more reports simply due to broader use. About CAERS →

Other ingredients

Gelatin · Magnesium Stearate · Silicon Dioxide · Microcrystalline Cellulose · Candurin Silver