DailyMed label
Diatrol
DailyMed label · PureTek Corporation · version 4
Key facts
| Product | Diatrol |
|---|---|
| Labeler | PureTek Corporation |
| Document type | HUMAN PRESCRIPTION DRUG LABEL |
| Active ingredients | .ALPHA.-TOCOPHEROL ACETATE, DL-, ARGININE HYDROCHLORIDE, ASCORBIC ACID, BIOTIN, CHOLECALCIFEROL, CHROMIUM NICOTINATE, GYMNEMA SYLVESTRE LEAF, LEVOMEFOLATE CALCIUM, METHYLCOBALAMIN, NIACINAMIDE, PANTOTHENIC ACID, PHYTONADIONE and 5 more |
| Active ingredient UNIIs | 19F5HK2737, 1C6V77QF41, 25X51I8RD4, 2ZK6ZS8392, 68Y4CF58BV, 6DU9Y533FA, 6SO6U10H04, 81G40H8B0T, 8K0I04919X, A034SE7857, A150AY412V, A9R10K3F2F and 5 more |
| Route | ORAL |
| NDC package codes | 59088-162-54 |
| Effective date | Aug 27, 2026 |
| Set ID | 0fe2b1cf-9085-ea65-e063-6294a90a80a6 |
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: