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LET ME CLARIFY - 49520-103-31 - (SALICYLIC ACID)

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Drug Information of LET ME CLARIFY

Product NDC: 49520-103
Proprietary Name: LET ME CLARIFY
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 LET ME CLARIFY

Product NDC: 49520-103
Labeler Name: mybody
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: part333D
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20120924

Package Information of LET ME CLARIFY

Package NDC: 49520-103-31
Package Description: 5 mL in 1 TUBE (49520-103-31)

NDC Information of LET ME CLARIFY

NDC Code 49520-103-31
Proprietary Name LET ME CLARIFY
Package Description 5 mL in 1 TUBE (49520-103-31)
Product NDC 49520-103
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name SALICYLIC ACID
Dosage Form Name GEL
Route Name TOPICAL
Start Marketing Date 20120924
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name mybody
Substance Name SALICYLIC ACID
Strength Number 2
Strength Unit g/100mL
Pharmaceutical Classes

Complete Information of LET ME CLARIFY


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