NDC 62032-522

NU-DERM SYSTEM NORMAL-DRY SKIN TRANSFORMATION TRIAL

Hydroquinone, Octinoxate,and Zinc Oxide

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

Product ID62032-522_25fd5bb4-16d0-408c-b0dd-5e6981f225d7
NDC62032-522
Product TypeHuman Prescription Drug
Proprietary NameNU-DERM SYSTEM NORMAL-DRY SKIN TRANSFORMATION TRIAL
Generic NameHydroquinone, Octinoxate,and Zinc Oxide
Dosage FormKit
Marketing Start Date2013-04-15
Marketing CategoryUNAPPROVED DRUG OTHER / UNAPPROVED DRUG OTHER
Labeler NameOMP, INC.
Active Ingredient Strength0
NDC Exclude FlagE
Listing Certified Through2018-12-31

Packaging

NDC 62032-522-60

1 KIT in 1 CARTON (62032-522-60) * 28 g in 1 BOTTLE, PLASTIC * 59 mL in 1 BOTTLE, PLASTIC * 59 mL in 1 BOTTLE, PLASTIC * 28 g in 1 TUBE * 28 g in 1 BOTTLE, PLASTIC * 28 g in 1 BOTTLE, PLASTIC
Marketing Start Date2013-04-15
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 62032-522-60 [62032052260]

nu-derm system normal-dry skin transformation trial KIT
Marketing CategoryUnapproved drug other
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2013-04-15

Drug Details

OpenFDA Data

SPL SET ID:b47c6867-ea72-443a-a6f1-6c122124f0fb
Manufacturer
RxNorm Concept Unique ID - RxCUI
  • 197795

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

    NDCBrand NameGeneric Name
    62032-516NU-DERM SYSTEM NORMAL-DRY SKIN TRANSFORMATION TRIALNU-DERM SYSTEM NORMAL-DRY SKIN TRANSFORMATION TRIAL
    62032-532NU-DERM system NORMAL-DRY SKIN TRANSFORMATION TRIALNU-DERM system NORMAL-DRY SKIN TRANSFORMATION TRIAL
    62032-514NU-DERM SYSTEM NORMAL-DRYHydroquinone, Octinoxate,and Zinc Oxide
    62032-522NU-DERM SYSTEM NORMAL-DRYHydroquinone, Octinoxate,and Zinc Oxide
    © 2025 FDA.report
    This site is not affiliated with or endorsed by the FDA.