NDC product
Clear Eyes Maximum Itchy Eye Relief
NDC 67172-999 · Prestige Brands Holdings, Inc.
Key facts
| Product NDC | 67172-999 |
|---|---|
| Proprietary name | Clear Eyes Maximum Itchy Eye Relief |
| Nonproprietary name | Glycerin and Naphazoline Hydrochloride and Zinc Sulfate |
| Substances | GLYCERIN, NAPHAZOLINE HYDROCHLORIDE, ZINC SULFATE |
| Dosage form | LIQUID |
| Route | OPHTHALMIC |
| Labeler | Prestige Brands Holdings, Inc. |
| Product type | HUMAN OTC DRUG |
| Marketing category | OTC MONOGRAPH DRUG |
| Application number | M018 |
| Pharmacologic classes | Allergens [CS], Cell-mediated Immunity [PE], Copper Absorption Inhibitor [EPC], Decreased Copper Ion Absorption [PE], Glycerol [CS], Increased Histamine Release [PE] and 2 more |
| Marketing start | Mar 15, 2011 |
| 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: