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NU-DERM STARTER SET NORMAL-DRY - 62032-504-00 - (Hydroquinone, Octinoxate, Oxybenzone and Zinc Oxide)

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Drug Information of NU-DERM STARTER SET NORMAL-DRY

Product NDC: 62032-504
Proprietary Name: NU-DERM STARTER SET NORMAL-DRY
Non Proprietary Name: Hydroquinone, Octinoxate, Oxybenzone and Zinc Oxide
Active Ingredient(s):    & nbsp;   Hydroquinone, Octinoxate, Oxybenzone and Zinc Oxide
Administration Route(s):
Dosage Form(s): KIT
Coding System: National Drug Codes(NDC)

Labeler Information of NU-DERM STARTER SET NORMAL-DRY

Product NDC: 62032-504
Labeler Name: OMP, INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number:
Marketing Category: UNAPPROVED DRUG OTHER
Start Marketing Date: 20070820

Package Information of NU-DERM STARTER SET NORMAL-DRY

Package NDC: 62032-504-00
Package Description: 1 KIT in 1 CARTON (62032-504-00) * 200 mL in 1 BOTTLE, PLASTIC * 57 g in 1 BOTTLE, PLASTIC * 200 mL in 1 BOTTLE, PLASTIC * 57 g in 1 BOTTLE, PLASTIC (62032-116-36) * 30 mL in 1 BOTTLE, PLASTIC (62032-200-10) * 57 g in 1 BOTTLE, PLASTIC (62032-101-36) * 57 g in 1 BOTTLE, PLASTIC (62032-100-36)

NDC Information of NU-DERM STARTER SET NORMAL-DRY

NDC Code 62032-504-00
Proprietary Name NU-DERM STARTER SET NORMAL-DRY
Package Description 1 KIT in 1 CARTON (62032-504-00) * 200 mL in 1 BOTTLE, PLASTIC * 57 g in 1 BOTTLE, PLASTIC * 200 mL in 1 BOTTLE, PLASTIC * 57 g in 1 BOTTLE, PLASTIC (62032-116-36) * 30 mL in 1 BOTTLE, PLASTIC (62032-200-10) * 57 g in 1 BOTTLE, PLASTIC (62032-101-36) * 57 g in 1 BOTTLE, PLASTIC (62032-100-36)
Product NDC 62032-504
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Hydroquinone, Octinoxate, Oxybenzone and Zinc Oxide
Dosage Form Name KIT
Route Name
Start Marketing Date 20070820
Marketing Category Name UNAPPROVED DRUG OTHER
Labeler Name OMP, INC.
Substance Name
Strength Number
Strength Unit
Pharmaceutical Classes

Complete Information of NU-DERM STARTER SET NORMAL-DRY


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