NDC 51224-153

Aluminum Acetate Astringent

Calcium Acetate And Aluminum Sulfate

Aluminum Acetate Astringent is a Topical Powder, For Solution in the Human Otc Drug category. It is labeled and distributed by Tagi Pharma Incorporated. The primary component is Calcium Acetate; Aluminum Sulfate.

Product ID51224-153_a4b9d3a3-fe12-4313-922f-abc93f440e6c
NDC51224-153
Product TypeHuman Otc Drug
Proprietary NameAluminum Acetate Astringent
Generic NameCalcium Acetate And Aluminum Sulfate
Dosage FormPowder, For Solution
Route of AdministrationTOPICAL
Marketing Start Date2011-06-15
Marketing CategoryOTC MONOGRAPH FINAL / OTC MONOGRAPH FINAL
Application Numberpart347
Labeler NameTAGI Pharma Incorporated
Substance NameCALCIUM ACETATE; ALUMINUM SULFATE
Active Ingredient Strength839 mg/2030mg; mg/2030mg
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 51224-153-24

12 BOX in 1 CARTON (51224-153-24) > 12 POUCH in 1 BOX (51224-153-12) > 2030 mg in 1 POUCH (51224-153-99)
Marketing Start Date2011-06-15
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 51224-153-12 [51224015312]

Aluminum Acetate Astringent POWDER, FOR SOLUTION
Marketing CategoryOTC MONOGRAPH FINAL
Application Numberpart347
Product TypeHUMAN OTC DRUG
Billing UnitEA
Marketing Start Date2011-06-15

NDC 51224-153-24 [51224015324]

Aluminum Acetate Astringent POWDER, FOR SOLUTION
Marketing CategoryOTC MONOGRAPH FINAL
Application Numberpart347
Product TypeHUMAN OTC DRUG
Billing UnitEA
Marketing Start Date2011-06-15

NDC 51224-153-99 [51224015399]

Aluminum Acetate Astringent POWDER, FOR SOLUTION
Marketing CategoryOTC MONOGRAPH FINAL
Application Numberpart347
Product TypeHUMAN OTC DRUG
Billing UnitEA
Marketing Start Date2011-06-15

Drug Details

Active Ingredients

IngredientStrength
CALCIUM ACETATE839 mg/2030mg

OpenFDA Data

SPL SET ID:6ebed2f4-6a06-47a3-bde4-c47b32cd81cb
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 1292923
    • © 2024 FDA.report
    This site is not affiliated with or endorsed by the FDA.