Diphenhydramine Hydrochloride And Zinc Acetate 51672-2089-02
- Manufacturer
- Sun Pharmaceutical Industries, Inc.
- Dosage Form
- Cream
- Route
- Topical
- Product Type
- Human Otc Drug
- Marketing Start
- September 20, 2005
- Listing Expires
- December 31, 2026
- Application
- M017
Active Ingredients
| Ingredient | Strength |
|---|---|
| Diphenhydramine Hydrochloride | 20 mg/g |
| Zinc Acetate | 1 mg/g |
Drug Class
Copper Absorption Inhibitor [EPC]Decreased Copper Ion Absorption [PE]Histamine H1 Receptor Antagonists [MoA]
Selected Package
51672-2089-02Selected1 TUBE in 1 CARTON (51672-2089-2) / 28.4 g in 1 TUBE