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NU-DERM SYSTEM NORMAL-OILY - 62032-515-60 - (Hydroquinone, Octinoxate, and Zinc Oxide)

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Drug Information of NU-DERM SYSTEM NORMAL-OILY

Product NDC: 62032-515
Proprietary Name: NU-DERM SYSTEM NORMAL-OILY
Non Proprietary Name: Hydroquinone, Octinoxate, and Zinc Oxide
Active Ingredient(s):    & nbsp;   Hydroquinone, Octinoxate, and Zinc Oxide
Administration Route(s):
Dosage Form(s): KIT
Coding System: National Drug Codes(NDC)

Labeler Information of NU-DERM SYSTEM NORMAL-OILY

Product NDC: 62032-515
Labeler Name: OMP, INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number:
Marketing Category: UNAPPROVED DRUG OTHER
Start Marketing Date: 20121107

Package Information of NU-DERM SYSTEM NORMAL-OILY

Package NDC: 62032-515-60
Package Description: 1 KIT in 1 CARTON (62032-515-60) * 59 mL in 1 BOTTLE, PLASTIC * 28.5 g in 1 BOTTLE, PLASTIC (62032-100-10) * 28 g in 1 BOTTLE, PLASTIC * 57 g in 1 BOTTLE, PLASTIC (62032-101-36) * 59 mL in 1 BOTTLE, PLASTIC * 28 g in 1 TUBE (62032-104-10)

NDC Information of NU-DERM SYSTEM NORMAL-OILY

NDC Code 62032-515-60
Proprietary Name NU-DERM SYSTEM NORMAL-OILY
Package Description 1 KIT in 1 CARTON (62032-515-60) * 59 mL in 1 BOTTLE, PLASTIC * 28.5 g in 1 BOTTLE, PLASTIC (62032-100-10) * 28 g in 1 BOTTLE, PLASTIC * 57 g in 1 BOTTLE, PLASTIC (62032-101-36) * 59 mL in 1 BOTTLE, PLASTIC * 28 g in 1 TUBE (62032-104-10)
Product NDC 62032-515
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Hydroquinone, Octinoxate, and Zinc Oxide
Dosage Form Name KIT
Route Name
Start Marketing Date 20121107
Marketing Category Name UNAPPROVED DRUG OTHER
Labeler Name OMP, INC.
Substance Name
Strength Number
Strength Unit
Pharmaceutical Classes

Complete Information of NU-DERM SYSTEM NORMAL-OILY


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