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Syntrax

Nectar Pink Grapefruit

Serving
7 Gram(s)
Per container
4
Form
powder
UPC
893912124595
DSLD
67404
Formula hash
7e84ac25474f
Brand context
Syntrax
Catalog
264
products
With avoid flag
16
products
FDA recalls
0
history
CAERS
1
reports
Caution-flaggedObjective label signals
Flagged excipients
2
0 avoid · 2 caution
FDA recalls
0
no recall history
CAERS reports
1
FDA consumer events
Certifications
0
none recorded
2 excipients carry authority-caution citations. · Every flag below links to the authority's published citation.

Supplement Facts

13 active ingredients
IngredientAmount% DV
Calories
otherUNII · 1
25 Calorie(s)—
Total Fat
Fat (unspecified)other
0 Gram(s)0%
Cholesterol
otherUNII · 97C5T2UQ7J
0 mg0%
Sodium
mineralUNII · 9NEZ333N27
15 mg1%
Potassium
mineralUNII · RWP5GA015D
3 effects
40 mg1%
Total Carbohydrates
CarbohydrateotherUNII · 0
0 Gram(s)0%
Protein
Protein (unspecified)other
6 Gram(s)12%
Vitamin A
vitaminUNII · 81G40H8B0T
UL · set3 effects
0 NP0%
Vitamin C
vitaminUNII · PQ6CK8PD0R
UL · set5 effects
0 NP0%
Calcium
mineralUNII · SY7Q814VUP
UL · set6 effects
0 NP2%
Iron
mineralUNII · E1UOL152H7
UL · set5 effects
0 NP0%
Phosphorus
mineralUNII · 27YLU75U4W
UL · set2 effects
0 NP2%
Magnesium
mineralUNII · I38ZP9992A
UL · set6 effects
0 NP0%
What this product supports · authorized claims

19 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

2 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 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 →
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

Whey Protein isolate · Citric Acid · Natural and Artificial flavors · Soy Lecithin · Acesulfame-K · Sucralose

Chemically equivalent

Same formula, different brand

Products with identical sorted (ingredient, amount) tuples.