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Antiperspirant - 53329-010-13 - (aluminum chlorohydrate)

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Drug Information of Antiperspirant

Product NDC: 53329-010
Proprietary Name: Antiperspirant
Non Proprietary Name: aluminum chlorohydrate
Active Ingredient(s): 13    mL/100mL & nbsp;   aluminum chlorohydrate
Administration Route(s): TOPICAL
Dosage Form(s): SPRAY
Coding System: National Drug Codes(NDC)

Labeler Information of Antiperspirant

Product NDC: 53329-010
Labeler Name: Medline Industries, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: part350
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20100601

Package Information of Antiperspirant

Package NDC: 53329-010-13
Package Description: 59 mL in 1 BOTTLE, SPRAY (53329-010-13)

NDC Information of Antiperspirant

NDC Code 53329-010-13
Proprietary Name Antiperspirant
Package Description 59 mL in 1 BOTTLE, SPRAY (53329-010-13)
Product NDC 53329-010
Product Type Name HUMAN OTC DRUG
Non Proprietary Name aluminum chlorohydrate
Dosage Form Name SPRAY
Route Name TOPICAL
Start Marketing Date 20100601
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Medline Industries, Inc.
Substance Name ALUMINUM CHLOROHYDRATE
Strength Number 13
Strength Unit mL/100mL
Pharmaceutical Classes

Complete Information of Antiperspirant


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