NDC 62032-514

NU-DERM SYSTEM NORMAL-DRY SKIN TRANSFORMATION

Hydroquinone, Octinoxate,and Zinc Oxide

NU-DERM SYSTEM NORMAL-DRY SKIN TRANSFORMATION is a Kit in the Human Prescription Drug category. It is labeled and distributed by Omp, Inc.. The primary component is .

Product ID62032-514_53845d82-8e3c-4498-89e0-1568174f8524
NDC62032-514
Product TypeHuman Prescription Drug
Proprietary NameNU-DERM SYSTEM NORMAL-DRY SKIN TRANSFORMATION
Generic NameHydroquinone, Octinoxate,and Zinc Oxide
Dosage FormKit
Marketing Start Date2012-11-07
Marketing CategoryUNAPPROVED DRUG OTHER / UNAPPROVED DRUG OTHER
Labeler NameOMP, INC.
Active Ingredient Strength0
NDC Exclude FlagE
Listing Certified Through2018-12-31

Packaging

NDC 62032-514-00

1 KIT in 1 CARTON (62032-514-00) * 198 mL in 1 BOTTLE, PLASTIC * 57 g in 1 BOTTLE, PLASTIC * 198 mL in 1 BOTTLE, PLASTIC * 48 g in 1 BOTTLE, PLASTIC * 85 g in 1 TUBE (62032-104-90) * 57 g in 1 BOTTLE, PLASTIC (62032-101-36) * 57 g in 1 BOTTLE, PLASTIC (62032-100-36)
Marketing Start Date2012-11-07
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 62032-514-00 [62032051400]

NU-DERM SYSTEM NORMAL-DRY SKIN TRANSFORMATION KIT
Marketing CategoryUnapproved drug other
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2012-11-07
Inactivation Date2020-01-31

Drug Details

OpenFDA Data

SPL SET ID:7e70faa2-ce6a-4815-9fa1-43c7025d80e6
Manufacturer
RxNorm Concept Unique ID - RxCUI
  • 197795

    • NDC Crossover Matching brand name "NU-DERM SYSTEM NORMAL-DRY SKIN TRANSFORMATION" or generic name "Hydroquinone, Octinoxate,and Zinc Oxide"

    NDCBrand NameGeneric Name
    62032-520NU-DERM SYSTEM NORMAL-DRY SKIN TRANSFORMATIONNU-DERM SYSTEM NORMAL-DRY SKIN TRANSFORMATION
    62032-529nu-derm system normal-dry skin transformationnu-derm system normal-dry skin transformation
    62032-514NU-DERM SYSTEM NORMAL-DRYHydroquinone, Octinoxate,and Zinc Oxide
    62032-522NU-DERM SYSTEM NORMAL-DRYHydroquinone, Octinoxate,and Zinc Oxide
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