21st Century

Cranberry Plus Probiotic

Serving
2 Tablet(s)
Per container
30
Form
tablet
UPC
740985278482
DSLD
Formula hash
4bbf9a1b1c6f
Brand context
Catalog
798
products
With avoid flag
196
products
FDA recalls
0
history
CAERS
3
reports
Avoid-flaggedObjective label signals
Flagged excipients
3
1 avoid · 2 caution
FDA recalls
0
no recall history
CAERS reports
3
FDA consumer events
Certifications
0
none recorded
1 avoid-level excipient · Every flag below links to the authority's published citation.

Supplement Facts

8 active ingredients
IngredientAmount% DV
Calories
otherUNII · 1
5 Calorie(s)
Total Carbohydrates
CarbohydrateotherUNII · 0
1 Gram(s)1%
Total Carbohydrates
CarbohydrateotherUNII · 0
1 Gram(s)2%
Calories
otherUNII · 1
0.5 Gram(s)
Vitamin C
vitaminUNII · PQ6CK8PD0R
UL · set5 effects
60 mg67%
Calcium
mineralUNII · SY7Q814VUP
UL · set6 effects
110 mg8%
Cranberry powder
cranberryherbUNII · 0MVO31Q3QS
500 mg
Probiotic Proprietary Blend
Proprietary Blend (non-nutrient/non-botanical)other
30 mg
What this product supports · authorized claims

11 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

  • ● 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 Blue #2 Carmine
    color

    Banned from direct food use in Norway; restricted in EU under Commission Regulation 1333/2008. FDA permits under 21 CFR 74.102 with labeling requirement.

  • ◐ 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).

FDA CAERS · adverse event context
3
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

Cellulose · Stearic Acid · Silicon Dioxide · Croscarmellose Sodium · Inulin · Magnesium Silicate · Magnesium Stearate · Polyethylene Glycol · Polyvinyl Alcohol