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Detoxify

Instant Clean Herbal Cleanse

Serving
4 Capsule(s)
Per container
3
Form
capsule-unknown
DSLD
321647
Formula hash
aa1510a743c1
Brand context
Detoxify
CA
Catalog
41
products
With avoid flag
1
products
FDA recalls
0
history
CAERS
1
reports
Avoid-flaggedObjective label signals
Flagged excipients
7
2 avoid · 5 caution
FDA recalls
0
no recall history
CAERS reports
1
FDA consumer events
Certifications
0
none recorded
2 avoid-level excipients · Every flag below links to the authority's published citation.

Supplement Facts

20 active ingredients
IngredientAmount% DV
Vitamin A
vitaminUNII · 81G40H8B0T
UL · set3 effects
750 mcg83%
Vitamin D
vitaminUNII · 9VU1KI44GP
UL · set4 effects
5 mcg25%
Thiamine
ThiaminvitaminUNII · X66NSO3N35
3 effects
0.8 mg67%
Riboflavin
vitaminUNII · TLM2976OFR
5 effects
0.9 mg69%
Niacin
vitaminUNII · 2679MF687A
UL · set3 effects
10 mg63%
Vitamin B6
vitaminUNII · KV2JZ1BI6Z
UL · set6 effects
1 mg59%
Folate
vitaminUNII · 935E97BOY8
UL · set2 effects
333 mcg DFE83%
Vitamin B12
vitaminUNII · 8406EY2OQA
3 effects
3 mcg125%
Biotin
vitaminUNII · 6SO6U10H04
3 effects
150 mcg500%
Pantothenic Acid
Pantothenic Acid (Vitamin B5)vitaminUNII · 19F5HK2737
5 mg100%
Calcium
mineralUNII · SY7Q814VUP
UL · set6 effects
200 mg15%
Magnesium
mineralUNII · I38ZP9992A
UL · set6 effects
80 mg19%
Zinc
mineralUNII · J41CSQ7QDS
UL · set8 effects
7.5 mg68%
Selenium
mineralUNII · H6241UJ22B
UL · set3 effects
35 mcg64%
Manganese
mineralUNII · 42Z2K6ZL8P
UL · set2 effects
1 mg43%
Chromium
mineralUNII · 0R0008Q3JB
1 effect
60 mcg171%
Creatine Monohydrate
CreatineherbUNII · 9603LN7R2Q
610 mg—
Proprietary Herb Blend
Proprietary Blend (Herb/Botanical)other
585 mg—
Taurine
herbUNII · 1EQV5MLY3D
400 mg—
Guarana
herbUNII · C21GE7524R
250 mg—
What this product supports · authorized claims

24 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

7 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 →
  • ● 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 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 Yellow 5
    color

    EU requires warning label 'may have an adverse effect on activity and attention in children' per Commission Regulation 1333/2008 Annex III (following Southampton study 2007). FDA requires specific label declaration (21 CFR 74.705).

    eur-lex.europa.eu →ecfr.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 5
    color

    EU requires warning label 'may have an adverse effect on activity and attention in children' per Commission Regulation 1333/2008 Annex III (following Southampton study 2007). FDA requires specific label declaration (21 CFR 74.705).

    eur-lex.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 →
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 · Gelatin · Gelatin · Magnesium Stearate · Brown Rice Flour