NDC product
Menstrual Relief Maximum Strength
NDC 41163-390 · United Natural Foods, Inc. dba UNFI
Key facts
| Product NDC | 41163-390 |
|---|---|
| Proprietary name | Menstrual Relief |
| Nonproprietary name | Acetaminophen, Caffeine and Pyrilamine maleate |
| Substances | ACETAMINOPHEN, CAFFEINE, PYRILAMINE MALEATE |
| Dosage form | TABLET, FILM COATED |
| Route | ORAL |
| Labeler | United Natural Foods, Inc. dba UNFI |
| Product type | HUMAN OTC DRUG |
| Marketing category | OTC MONOGRAPH DRUG |
| Application number | M013 |
| Pharmacologic classes | Central Nervous System Stimulant [EPC], Central Nervous System Stimulation [PE], Methylxanthine [EPC], Xanthines [CS] |
| Marketing start | Apr 29, 2002 |
| Marketing end | Feb 28, 2027 |
At a glance
- 1–9 Package NDCs
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About National Drug Codes (NDC)
The National Drug Code (NDC) is the FDA's product identifier for drugs; the product NDC identifies the labeler and product, and each package adds a package code.
Source: U.S. Food and Drug Administration (FDA), National Drug Code Directory