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High T

High T Women

Serving
2 Capsule(s)
Per container
30
Form
capsule-unknown
UPC
851806004248
DSLD
181665
Formula hash
409170b0d60a
Brand context
High T
Catalog
20
products
With avoid flag
20
products
FDA recalls
0
history
CAERS
5
reports
Avoid-flaggedObjective label signals
Flagged excipients
5
1 avoid · 4 caution
FDA recalls
0
no recall history
CAERS reports
5
FDA consumer events
Certifications
0
none recorded
1 avoid-level excipient · Every flag below links to the authority's published citation.

Supplement Facts

7 active ingredients
IngredientAmount% DV
Vitamin E
vitaminUNII · H4N855PNZ1
UL · set1 effect
30 IU100%
Niacin
vitaminUNII · 2679MF687A
UL · set3 effects
4 mg20%
Vitamin B6
vitaminUNII · KV2JZ1BI6Z
UL · set6 effects
8 mg400%
Vitamin B12
vitaminUNII · 8406EY2OQA
3 effects
48 mcg8%
Zinc
mineralUNII · J41CSQ7QDS
UL · set8 effects
1.5 mg10%
HMRlignan
Hemlock spruceherb
30 mg—
HighT Proprietary Blend
Proprietary Blend (Combination)other
900 mg—
What this product supports · authorized claims

13 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

5 flagged · authority citations

  • ● AVOIDTitanium Dioxide
    color

    Banned in EU food products effective 2022-08 (Commission Regulation (EU) 2022/63) following EFSA Panel opinion that a safe daily intake could not be established due to genotoxicity concerns. Still GRAS in the US under 21 CFR 73.575 but EU position is stricter.

    eur-lex.europa.eu →efsa.europa.eu →ecfr.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 →
  • ◐ 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 Yellow #6
    color

    EU requires 'attention in children' warning per Reg 1333/2008 Annex III (Southampton study 2007). Banned in Norway + Finland; allowed in US under 21 CFR 74.706 with declaration.

    eur-lex.europa.eu →
FDA CAERS · adverse event context
5
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 · Cellulose

Chemically equivalent

Same formula, different brand

Products with identical sorted (ingredient, amount) tuples.