Anti-itch - 53329-091-91 - (hydrocortisone)

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Drug Information of Anti-itch

Product NDC: 53329-091
Proprietary Name: Anti-itch
Non Proprietary Name: hydrocortisone
Active Ingredient(s): 10    mg/g & nbsp;   hydrocortisone
Administration Route(s): TOPICAL
Dosage Form(s): CREAM
Coding System: National Drug Codes(NDC)

Labeler Information of Anti-itch

Product NDC: 53329-091
Labeler Name: Medline Industries, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: part348
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20100301

Package Information of Anti-itch

Package NDC: 53329-091-91
Package Description: 48 PACKET in 1 CARTON (53329-091-91) > 1.5 g in 1 PACKET (53329-091-90)

NDC Information of Anti-itch

NDC Code 53329-091-91
Proprietary Name Anti-itch
Package Description 48 PACKET in 1 CARTON (53329-091-91) > 1.5 g in 1 PACKET (53329-091-90)
Product NDC 53329-091
Product Type Name HUMAN OTC DRUG
Non Proprietary Name hydrocortisone
Dosage Form Name CREAM
Route Name TOPICAL
Start Marketing Date 20100301
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name Medline Industries, Inc.
Substance Name HYDROCORTISONE
Strength Number 10
Strength Unit mg/g
Pharmaceutical Classes

Complete Information of Anti-itch


General Information