NDC 10481-3012

POTASSIUM HYDROXIDE

Potassium Hydroxide

POTASSIUM HYDROXIDE is a Topical Liquid in the Human Prescription Drug category. It is labeled and distributed by Gordon Laboratories. The primary component is Potassium Hydroxide.

Product ID10481-3012_fdb68978-98c7-4814-abd3-df3d329a77d5
NDC10481-3012
Product TypeHuman Prescription Drug
Proprietary NamePOTASSIUM HYDROXIDE
Generic NamePotassium Hydroxide
Dosage FormLiquid
Route of AdministrationTOPICAL
Marketing Start Date2010-07-16
Marketing CategoryUNAPPROVED DRUG OTHER / UNAPPROVED DRUG OTHER
Labeler NameGordon Laboratories
Substance NamePOTASSIUM HYDROXIDE
Active Ingredient Strength0 g/g
NDC Exclude FlagE
Listing Certified Through2017-12-31

Packaging

NDC 10481-3012-1

59 g in 1 BOTTLE, GLASS (10481-3012-1)
Marketing Start Date2010-07-16
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 10481-3012-1 [10481301201]

POTASSIUM HYDROXIDE LIQUID
Marketing Categoryunapproved drug other
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitML
Marketing Start Date2010-07-16
Inactivation Date2019-10-29

Drug Details

Active Ingredients

IngredientStrength
POTASSIUM HYDROXIDE.05 g/g

OpenFDA Data

SPL SET ID:6eeb7bf1-cfd6-4574-94bb-ff69ec91359f
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 312538
  • UPC Code
  • 0850217001785
  • NDC Crossover Matching brand name "POTASSIUM HYDROXIDE" or generic name "Potassium Hydroxide"

    NDCBrand NameGeneric Name
    10481-3012POTASSIUM HYDROXIDEPOTASSIUM HYDROXIDE
    79659-001MIRACLE WATER 3 in 1Potassium hydroxide
    70970-002OHTrust Nano Ion WaterPotassium hydroxide
    70970-100OHTrust Nano Ion WaterPotassium hydroxide

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