DailyMed label
Finazol
DailyMed label · PureTek Corporation · version 2
Key facts
| Product | Finazol |
|---|---|
| Labeler | PureTek Corporation |
| Document type | HUMAN PRESCRIPTION DRUG LABEL |
| Active ingredients | .ALPHA.-TOCOPHEROL ACETATE, DL-, ASCORBIC ACID, BIOTIN, BORON, CALCIUM CARBONATE, CHOLECALCIFEROL, CHROMIUM NICOTINATE, CUPROUS OXIDE, FERROUS FUMARATE, LEVOMEFOLATE CALCIUM, MAGNESIUM OXIDE, MANGANESE SULFATE and 12 more |
| Active ingredient UNIIs | 19F5HK2737, 1C4QK22F9J, 1C6V77QF41, 25X51I8RD4, 3A3U0GI71G, 3LE3D9D6OY, 660YQ98I10, 68Y4CF58BV, 6SO6U10H04, 81AH48963U, 8K0I04919X, A150AY412V and 12 more |
| Route | ORAL |
| NDC package codes | 59088-008-54 |
| Effective date | Nov 7, 2024 |
| Set ID | 24290823-022a-433b-e063-6394a90a8fd0 |
At a glance
- 1–9 NDC package codes
- 10–99 Active ingredients
- None Manufacturing establishments listed
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About DailyMed drug labels
DailyMed publishes the structured product labeling (SPL) that companies submit to the FDA, including package NDCs, ingredients and the establishments that make each product.
Source: U.S. National Library of Medicine (NLM), DailyMed · Source date: