NDC 51672-2089 – Diphenhydramine Hydrochloride and Zinc Acetate
Diphenhydramine Hydrochloride 20 mg/g; Zinc Acetate 1 mg/g · Cream · Topical
Product NDC51672-2089
Product details
- Brand name
- Diphenhydramine Hydrochloride and Zinc Acetate
- Generic name
- Diphenhydramine Hydrochloride and Zinc Acetate
- Labeler
- Sun Pharmaceutical Industries, Inc.
- Dosage form
- Cream
- Route
- Topical
- Marketing category
- OTC MONOGRAPH DRUG · M017
- Marketed since
- September 20, 2005
- Listing expires
- December 31, 2026
- Pharmacologic class
- Copper Absorption Inhibitor; Histamine-1 Receptor Antagonist
Active ingredients
- Diphenhydramine Hydrochloride 20 mg/g
- Zinc Acetate 1 mg/g
Uses, dosage, side effects and warnings for Diphenhydramine Hydrochloride and Zinc Acetate →
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 51672-2089-2 | 1 TUBE in 1 CARTON (51672-2089-2) / 28.4 g in 1 TUBE | Sep 20, 2005 |
Other Diphenhydramine Hydrochloride and Zinc Acetate products
- 70677-1213 Diphenhydramine Hydrochloride 20 mg/g; Zinc Acetate 1 mg/g · Cream · STRATEGIC SOURCING SERVICES LLC