NDC 69968-0459 – Benadryl Extra Strength Itch Relief
Zinc Acetate 1 mg/mL; Diphenhydramine Hydrochloride 20 mg/mL · Solution · Topical
Product NDC69968-0459
Product details
- Brand name
- Benadryl Extra Strength Itch Relief
- Generic name
- DIPHENHYDRAMINE HYDROCHLORIDE and Zinc Acetate
- Labeler
- Kenvue Brands LLC
- Dosage form
- Solution
- Route
- Topical
- Marketing category
- OTC MONOGRAPH DRUG · M017
- Marketed since
- June 1, 2019
- Listing expires
- December 31, 2026
- Pharmacologic class
- Copper Absorption Inhibitor; Histamine-1 Receptor Antagonist
Active ingredients
- Zinc Acetate 1 mg/mL
- Diphenhydramine Hydrochloride 20 mg/mL
Uses, dosage, side effects and warnings for Benadryl Extra Strength Itch Relief →
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 69968-0459-1 | 1 APPLICATOR in 1 CARTON (69968-0459-1) / 14 mL in 1 APPLICATOR | Jun 1, 2019 |