NDC product
Refresh RELIEVA PF
NDC 0023-4515 · Allergan, Inc.
Key facts
| Product NDC | 0023-4515 |
|---|---|
| Proprietary name | Refresh RELIEVA PF |
| Nonproprietary name | Carboxymethylcellulose sodium and Glycerin |
| Substances | CARBOXYMETHYLCELLULOSE SODIUM, GLYCERIN |
| Dosage form | SOLUTION/ DROPS |
| Route | OPHTHALMIC |
| Labeler | Allergan, Inc. |
| Product type | HUMAN OTC DRUG |
| Marketing category | OTC MONOGRAPH DRUG |
| Application number | M018 |
| Pharmacologic classes | Allergens [CS], Cell-mediated Immunity [PE], Glycerol [CS], Increased Histamine Release [PE], Increased IgG Production [PE], Non-Standardized Chemical Allergen [EPC] |
| Marketing start | Sep 25, 2020 |
| Listing certified through | Dec 31, 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 · Source date: