NDC product
Refresh Digital PF
NDC 0023-6954 · Allergan, Inc.
Key facts
| Product NDC | 0023-6954 |
|---|---|
| Proprietary name | Refresh Digital PF |
| Nonproprietary name | Carboxymethylcellulose sodium, Glycerin and Polysorbate 80 |
| Substances | CARBOXYMETHYLCELLULOSE SODIUM, GLYCERIN, POLYSORBATE 80 |
| 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 | Aug 1, 2020 |
| Listing certified through | Dec 31, 2026 |
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: