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ELF Zit Eraser - 76354-017-01 - (SALICYLIC ACID)

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Drug Information of ELF Zit Eraser

Product NDC: 76354-017
Proprietary Name: ELF Zit Eraser
Non Proprietary Name: SALICYLIC ACID
Active Ingredient(s): 1    g/100g & nbsp;   SALICYLIC ACID
Administration Route(s): TOPICAL
Dosage Form(s): LIQUID
Coding System: National Drug Codes(NDC)

Labeler Information of ELF Zit Eraser

Product NDC: 76354-017
Labeler Name: J. A. Cosmetics U.S. INC
Product Type: HUMAN OTC DRUG
FDA Application Number: part358H
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20120129

Package Information of ELF Zit Eraser

Package NDC: 76354-017-01
Package Description: 4 g in 1 TUBE (76354-017-01)

NDC Information of ELF Zit Eraser

NDC Code 76354-017-01
Proprietary Name ELF Zit Eraser
Package Description 4 g in 1 TUBE (76354-017-01)
Product NDC 76354-017
Product Type Name HUMAN OTC DRUG
Non Proprietary Name SALICYLIC ACID
Dosage Form Name LIQUID
Route Name TOPICAL
Start Marketing Date 20120129
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name J. A. Cosmetics U.S. INC
Substance Name SALICYLIC ACID
Strength Number 1
Strength Unit g/100g
Pharmaceutical Classes

Complete Information of ELF Zit Eraser


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