58232-0741 : Benadryl Extra Strength Topical Cream


NDC: 58232-0741
Labeler: Johnson & Johnson Consumer Products Company, Division of Johnson & Johnson Consumer Companies, Inc.
Product Type: Human OTC Drug
Drug Name: Benadryl Extra Strength Itch Stopping
Dosage Form: Topical Cream
Application #: part348
Rev. Date: 


NDC Package Codes:

  • 58232-0741-1: 1 TUBE IN 1 CARTON (58232‑0741‑1) > 28.3 G IN 1 TUBE
  • 58232-0741-2: 1 TUBE IN 1 CARTON (58232‑0741‑2) > 36.9 G IN 1 TUBE

Active Ingredients:

  • Diphenhydramine Hydrochloride
  • Zinc Acetate

Dosage Strength:

  • 2 mg/g
  • 1 mg/g

Related Products:

Based on records with the same trade name.
  • 58232-0744 Benadryl Extra Strength Itch Stopping 20 mg/ml Topical Gel by Johnson & Johnson Consumer Products Company, Division of Johnson & Johnson Consumer Companies, Inc.
  • 69968-0223 Benadryl Extra Strength Topical Cream by Johnson & Johnson Consumer Inc.
  • 69968-0242 Benadryl Extra Strength Itch Stopping 20 mg/ml Topical Gel by Johnson & Johnson Consumer Inc.

NDC QR Code

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NDC 58232-0741 QR Code

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Note: The RxChat NDC Database uses publicly available data from the FDA and the U.S. National Library of Medicine (NLM); The NLM is not responsible for the data presented and does not endorse or recommend this or any other product. While we make every effort to ensure that the information presented is accurate, you should assume that all results are unvalidated. To report any errors or inconsistencies please contact us.