NDC 76271-001

DR. WALTONS BABY POWDER

Talc

DR. WALTONS BABY POWDER is a Topical Powder in the Human Otc Drug category. It is labeled and distributed by Dr. Waltons, Incorporated. The primary component is Alpha-tocopherol; Zinc Oxide.

Product ID76271-001_c6e98d27-268e-4ab6-98d6-746b45d4c56c
NDC76271-001
Product TypeHuman Otc Drug
Proprietary NameDR. WALTONS BABY POWDER
Generic NameTalc
Dosage FormPowder
Route of AdministrationTOPICAL
Marketing Start Date2011-07-09
Marketing CategoryOTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL
Application Numberpart347
Labeler NameDr. Waltons, Incorporated
Substance NameALPHA-TOCOPHEROL; ZINC OXIDE
Active Ingredient Strength5 g/675g; g/675g
NDC Exclude FlagE
Listing Certified Through2017-12-31

Packaging

NDC 76271-001-02

55 g in 1 BOTTLE, PLASTIC (76271-001-02)
Marketing Start Date2011-07-09
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 76271-001-24 [76271000124]

DR. WALTONS BABY POWDER POWDER
Marketing CategoryOTC monograph not final
Application Numberpart347
Product TypeHUMAN OTC DRUG
Marketing Start Date2011-07-09
Inactivation Date2019-11-13

NDC 76271-001-02 [76271000102]

DR. WALTONS BABY POWDER POWDER
Marketing CategoryOTC monograph not final
Application Numberpart347
Product TypeHUMAN OTC DRUG
Marketing Start Date2011-07-09
Inactivation Date2019-11-13

Drug Details

Active Ingredients

IngredientStrength
ALPHA-TOCOPHEROL5.2 g/675g

OpenFDA Data

SPL SET ID:4c0dac58-34b5-418a-a54c-5ffcb690771f
Manufacturer
UNII
UPC Code
  • 0850894003003
  • NDC Crossover Matching brand name "DR. WALTONS BABY POWDER" or generic name "Talc"

    NDCBrand NameGeneric Name
    0363-0901BabyTALC
    76271-001DR. WALTONSTALC
    52862-010Health Smart BabyTALC
    43749-112Natures Choice BabyTalc
    50346-004Pan Aromas BabyTALC
    63256-100SclerosolTalc
    66854-018SPAI-SONSTALC
    63256-200Sterile TalcTalc
    62327-222SteritalcTalc
    62327-333SteritalcTalc
    62327-444SteritalcTalc

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