NDC product
Zicam
NDC 10237-482 · Church & Dwight Co., Inc.
Key facts
| Product NDC | 10237-482 |
|---|---|
| Proprietary name | Zicam |
| Nonproprietary name | Allium cepa 5x, Zincum aceticum 2x, Zincum gluconium 1x |
| Substances | ZINC ACETATE ANHYDROUS, ONION, ZINC GLUCONATE |
| Dosage form | TABLET |
| Route | ORAL |
| Labeler | Church & Dwight Co., Inc. |
| Product type | HUMAN OTC DRUG |
| Marketing category | UNAPPROVED HOMEOPATHIC |
| Pharmacologic classes | Allergens [CS], Cell-mediated Immunity [PE], Copper Absorption Inhibitor [EPC], Decreased Copper Ion Absorption [PE], Dietary Proteins [CS], Increased Histamine Release [PE] and 2 more |
| Marketing start | Jun 1, 2026 |
| 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: