NDC product
Refill 3
NDC 50814-017 · GFA Production (Xiamen) Co., Ltd.
Key facts
| Product NDC | 50814-017 |
|---|---|
| Proprietary name | Refill 3 |
| Nonproprietary name | BENZALKONIUM CHLORIDE, LIDOCAINE HYDROCHLORIDE |
| Substances | BENZALKONIUM CHLORIDE, LIDOCAINE HYDROCHLORIDE |
| Dosage form | CREAM |
| Route | TOPICAL |
| Labeler | GFA Production (Xiamen) Co., Ltd. |
| Product type | HUMAN OTC DRUG |
| Marketing category | OTC MONOGRAPH DRUG |
| Application number | M003 |
| Pharmacologic classes | Amide Local Anesthetic [EPC], Amides [CS], Antiarrhythmic [EPC], Local Anesthesia [PE] |
| Marketing start | Aug 10, 2016 |
| 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: