NDC product
Rite Aid Ultra Zinc Cold Therapy
NDC 11822-1181 · RITE AID CORPORATION
Key facts
| Product NDC | 11822-1181 |
|---|---|
| Proprietary name | Rite Aid Ultra Zinc Cold Therapy |
| Nonproprietary name | Zincum Gluconicum |
| Substances | ZINC GLUCONATE |
| Dosage form | TABLET, CHEWABLE |
| Route | ORAL |
| Labeler | RITE AID CORPORATION |
| Product type | HUMAN OTC DRUG |
| Marketing category | UNAPPROVED HOMEOPATHIC |
| Pharmacologic classes | Copper Absorption Inhibitor [EPC], Decreased Copper Ion Absorption [PE] |
| Marketing start | Apr 15, 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: