NDC 65923-495

Family Care Anti-Itch

Diphenhydramine Hydrochloride Zinc Acetate

Family Care Anti-Itch is a Topical Cream in the Human Otc Drug category. It is labeled and distributed by United Exchange Corp.. The primary component is Diphenhydramine Hydrochloride; Zinc Acetate.

Product ID65923-495_bf06744c-d19e-49be-a34d-1c787367b51b
NDC65923-495
Product TypeHuman Otc Drug
Proprietary NameFamily Care Anti-Itch
Generic NameDiphenhydramine Hydrochloride Zinc Acetate
Dosage FormCream
Route of AdministrationTOPICAL
Marketing Start Date2014-11-24
Marketing CategoryOTC MONOGRAPH FINAL / OTC MONOGRAPH FINAL
Application Numberpart347
Labeler NameUnited Exchange Corp.
Substance NameDIPHENHYDRAMINE HYDROCHLORIDE; ZINC ACETATE
Active Ingredient Strength1 g/100g; g/100g
NDC Exclude FlagN
Listing Certified Through2019-12-31

Packaging

NDC 65923-495-28

1 TUBE in 1 CARTON (65923-495-28) > 28 g in 1 TUBE
Marketing Start Date2014-11-24
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 65923-495-28 [65923049528]

Family Care Anti-Itch CREAM
Marketing CategoryOTC monograph final
Application Numberpart347
Product TypeHUMAN OTC DRUG
Marketing Start Date2014-11-24
Inactivation Date2020-01-31

Drug Details

Active Ingredients

IngredientStrength
DIPHENHYDRAMINE HYDROCHLORIDE1 g/100g

OpenFDA Data

SPL SET ID:1fff5104-05ae-4ab2-882a-282b5de38bfe
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 1292313
  • UPC Code
  • 0831527004956
  • NDC Crossover Matching brand name "Family Care Anti-Itch" or generic name "Diphenhydramine Hydrochloride Zinc Acetate"

    NDCBrand NameGeneric Name
    65923-494Family Care Anti-ItchHydrocortisone
    65923-495Family Care Anti-ItchDiphenhydramine hydrochloride Zinc Acetate
    65923-925Family Care Anti-ItchHydrocortisone
    68169-0049FAMILY CARE ANTI-ITCHDIPHENHYDRAMINE HYDROCHLORIDE
    20276-325LuckyDiphenhydramine hydrochloride Zinc acetate
    47046-168LuckyDiphenhydramine hydrochloride Zinc acetate

    © 2024 FDA.report
    This site is not affiliated with or endorsed by the FDA.