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antiperspirant deodorant - 50636-003-65 - (ALUMINUM CHLOROHYDRATE)

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Drug Information of antiperspirant deodorant

Product NDC: 50636-003
Proprietary Name: antiperspirant deodorant
Non Proprietary Name: ALUMINUM CHLOROHYDRATE
Active Ingredient(s): 15    mL/100mL & nbsp;   ALUMINUM CHLOROHYDRATE
Administration Route(s): TOPICAL
Dosage Form(s): LIQUID
Coding System: National Drug Codes(NDC)

Labeler Information of antiperspirant deodorant

Product NDC: 50636-003
Labeler Name: Frabel S.A de C.V.
Product Type: HUMAN OTC DRUG
FDA Application Number: part350
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20100331

Package Information of antiperspirant deodorant

Package NDC: 50636-003-65
Package Description: 65 mL in 1 BOTTLE, WITH APPLICATOR (50636-003-65)

NDC Information of antiperspirant deodorant

NDC Code 50636-003-65
Proprietary Name antiperspirant deodorant
Package Description 65 mL in 1 BOTTLE, WITH APPLICATOR (50636-003-65)
Product NDC 50636-003
Product Type Name HUMAN OTC DRUG
Non Proprietary Name ALUMINUM CHLOROHYDRATE
Dosage Form Name LIQUID
Route Name TOPICAL
Start Marketing Date 20100331
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Frabel S.A de C.V.
Substance Name ALUMINUM CHLOROHYDRATE
Strength Number 15
Strength Unit mL/100mL
Pharmaceutical Classes

Complete Information of antiperspirant deodorant


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