Bayer
One A Day Women's 50+ Complete Multivitamin
LNHPD
26199303
Formula hash
c07434174522
Catalog
112
products
With avoid flag
5
products
FDA recalls
0
history
CAERS
2
reports
Clean labelObjective label signals
Flagged excipients
0
none
FDA recalls
0
no recall history
CAERS reports
1
FDA consumer events
Certifications
0
none recorded
No authority-flagged excipients or recalls. · Every flag below links to the authority's published citation.
Supplement Facts
12 active ingredients| Ingredient | Amount | % DV |
|---|---|---|
| Riboflavin vitaminUNII · TLM2976OFR 5 effects | 3.4 mg | — |
| Folate vitaminUNII · 935E97BOY8 UL · set2 effects | 400.0 Microgram | — |
| Iodine mineralUNII · 9679TC07X4 UL · set2 effects | 150.0 Microgram | — |
| Molybdenum mineralUNII · 81AH48963U UL · set1 effect | 90.0 Microgram | — |
| Niacin vitaminUNII · 2679MF687A UL · set3 effects | 20.0 mg | — |
| Vitamin A vitaminUNII · 81G40H8B0T UL · set3 effects | 2800.0 IU | — |
| Vitamin A vitaminUNII · 81G40H8B0T UL · set3 effects | 840.0 microgram RAE | — |
| Selenium mineralUNII · H6241UJ22B UL · set3 effects | 27.0 Microgram | — |
| Thiamine ThiaminvitaminUNII · X66NSO3N35 3 effects | 4.5 mg | — |
| Vitamin D vitaminUNII · 9VU1KI44GP UL · set4 effects | 1000.0 IU | — |
| Vitamin D vitaminUNII · 9VU1KI44GP UL · set4 effects | 25.0 Microgram | — |
| Pantothenic Acid Pantothenic Acid (Vitamin B5)vitaminUNII · 19F5HK2737 | 15.0 mg | — |
What this product supports · authorized claims
16 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.
- from: Niacin · Riboflavin · Thiamin
- from: Niacin · Riboflavin · Thiamin
- from: Thiamin
- from: Riboflavin · Vitamin A
- from: Folate
- from: Selenium · Vitamin A · Vitamin D
- from: Iodine · Selenium
- from: Vitamin D
- from: Vitamin D
- from: Vitamin D
- from: Vitamin A
- from: Molybdenum
- from: Iodine
- from: Niacin · Riboflavin
- from: Riboflavin · Selenium
- from: Folate
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 →