Cellucor

CLK

Serving
3 Softgel(s)
Per container
30
Form
capsule-unknown
DSLD
Formula hash
b4f92b692afe
Brand context
Catalog
476
products
With avoid flag
15
products
FDA recalls
0
history
CAERS
28
reports
Avoid-flaggedObjective label signals
Flagged excipients
5
1 avoid · 4 caution
FDA recalls
0
no recall history
CAERS reports
10
FDA consumer events
Certifications
0
none recorded
1 avoid-level excipient · Every flag below links to the authority's published citation.

Supplement Facts

6 active ingredients
IngredientAmount% DV
Calories
otherUNII · 1
25 {Calories}
Total Fat
Fat (unspecified)other
2 g3%
Conjugated Linoleic Acid
fatty_acidUNII · G199I91G4B
1.7 g
L-Carnitine
herbUNII · 0G389FZZ9M
500 mg
Razberi-K
Raspberry Ketonesherb
100 mg
7-Keto(R) DHEA
7-KETO-DHEAherb
100 mg
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.

  • ◐ 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.

  • ◐ 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).

  • ◐ 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).

  • ◐ 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.

FDA CAERS · adverse event context
10
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 · Glycerin · purified Water · Beeswax · Soy Lecithin · Natural and Artificial flavor · Silicon Dioxide

Chemically equivalent

Same formula, different brand

Products with identical sorted (ingredient, amount) tuples.