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Clearasil Ultra - 63824-381-03 - (Salicylic Acid)

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Drug Information of Clearasil Ultra

Product NDC: 63824-381
Proprietary Name: Clearasil Ultra
Non Proprietary Name: Salicylic Acid
Active Ingredient(s): 2    g/100mL & nbsp;   Salicylic Acid
Administration Route(s): TOPICAL
Dosage Form(s): GEL
Coding System: National Drug Codes(NDC)

Labeler Information of Clearasil Ultra

Product NDC: 63824-381
Labeler Name: Reckitt Benckiser LLC
Product Type: HUMAN OTC DRUG
FDA Application Number: part333D
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20120721

Package Information of Clearasil Ultra

Package NDC: 63824-381-03
Package Description: 3 mL in 1 PACKET (63824-381-03)

NDC Information of Clearasil Ultra

NDC Code 63824-381-03
Proprietary Name Clearasil Ultra
Package Description 3 mL in 1 PACKET (63824-381-03)
Product NDC 63824-381
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Salicylic Acid
Dosage Form Name GEL
Route Name TOPICAL
Start Marketing Date 20120721
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name Reckitt Benckiser LLC
Substance Name SALICYLIC ACID
Strength Number 2
Strength Unit g/100mL
Pharmaceutical Classes

Complete Information of Clearasil Ultra


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