Zipfizz
ZIPFIZZ ORANGE SODA
LNHPD
8880417
Catalog
14
products
With avoid flag
0
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
13 active ingredients| Ingredient | Amount | % DV |
|---|---|---|
| Magnesium mineralUNII · I38ZP9992A UL · set6 effects | 100.0 milligrams | — |
| Vitamin B12 vitaminUNII · 8406EY2OQA 3 effects | 0.98 micrograms | — |
| Zinc mineralUNII · J41CSQ7QDS UL · set8 effects | 7.5 milligrams | — |
| Beta-Carotene Vitamin AvitaminUNII · 01YAE03M7J UL · set3 effects | 1400.28 micrograms | — |
| 2-Aminoethanesulfonic Acid TaurineherbUNII · 5L08GE4332 | 100.0 milligrams | — |
| 1,2-dithiolane-3-pentanoic acid other | 5.0 milligrams | — |
| Copper mineralUNII · 789U1901C5 UL · set3 effects | 250.0 micrograms | — |
| Vitamin B12 vitaminUNII · 8406EY2OQA 3 effects | 2500.0 micrograms | — |
| Vitamin B12 vitaminUNII · 8406EY2OQA 3 effects | 2500.0 micrograms | — |
| Vitis vinifera Grapeherb | 2.5 milligrams | — |
| Vitis vinifera Grapeherb | — | — |
| Chromium mineralUNII · 0R0008Q3JB 1 effect | 60.0 micrograms | — |
| Riboflavin vitaminUNII · TLM2976OFR 5 effects | 0.85 milligrams | — |
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.
- from: Magnesium · Riboflavin · Vitamin B12
- from: Magnesium · Riboflavin
- from: Riboflavin · Vitamin A
- from: Vitamin B12
- from: Chromium
- from: Vitamin A · Zinc
- from: Copper · Vitamin A · Zinc
- from: Magnesium
- from: Magnesium · Zinc
- from: Magnesium
- from: Zinc
- from: Zinc
- from: Zinc
- from: Zinc
- from: Copper
- from: Copper
- from: Magnesium · Riboflavin
- from: Riboflavin · Zinc
- from: Vitamin B12
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 →