NDC 81335-532

ZCort Ultra

Hydrocortisone Acetate 1%

ZCort Ultra is a Topical Cream in the Human Otc Drug category. It is labeled and distributed by Rxdino, Llc. The primary component is Hydrocortisone Acetate.

• Product ID: 81335-532_b68f8ada-58e9-e8e4-e053-2a95a90ab02d
• NDC: 81335-532
• Product Type: Human Otc Drug
• Proprietary Name: ZCort Ultra
• Generic Name: Hydrocortisone Acetate 1%
• Dosage Form: Cream
• Route of Administration: TOPICAL
• Marketing Start Date: 2021-03-01
• Marketing Category: OTC MONOGRAPH NOT FINAL /
• Application Number: part348
• Labeler Name: RxDino, LLC
• Substance Name: HYDROCORTISONE ACETATE
• Active Ingredient Strength: 10 mg/g
• NDC Exclude Flag: N
• Listing Certified Through: 2022-12-31

Packaging

NDC 81335-532-15

15 g in 1 BOX (81335-532-15)

• Marketing Start Date: 2021-03-01
• NDC Exclude Flag: N
• Sample Package?: N

Drug Details

NDC Crossover Matching brand name "ZCort Ultra" or generic name "Hydrocortisone Acetate 1%"

NDC	Brand Name	Generic Name
71241-002	BIOCORNEUM ADVANCED SCAR TREATMENT ANTI-ITCH	Hydrocortisone acetate 1%
81335-532	ZCort	Hydrocortisone Acetate 1%