NDC 0096-0709

Xerac AC

Xerac Ac

Xerac AC is a Topical Liquid in the Human Otc Drug category. It is labeled and distributed by Person And Covey. The primary component is Aluminum Chloride.

Product ID0096-0709_7b713b7d-3d74-36f4-e053-2991aa0a839e
NDC0096-0709
Product TypeHuman Otc Drug
Proprietary NameXerac AC
Generic NameXerac Ac
Dosage FormLiquid
Route of AdministrationTOPICAL
Marketing Start Date1996-06-01
Marketing CategoryOTC MONOGRAPH FINAL / OTC MONOGRAPH FINAL
Application Numberpart350
Labeler NamePerson and Covey
Substance NameALUMINUM CHLORIDE
Active Ingredient Strength0 g/g
NDC Exclude FlagN
Listing Certified Through2019-12-31

Packaging

NDC 0096-0709-35

29.09 g in 1 PACKAGE (0096-0709-35)
Marketing Start Date1996-06-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 0096-0709-35 [00096070935]

Xerac AC LIQUID
Marketing CategoryOTC monograph final
Application Numberpart350
Product TypeHUMAN OTC DRUG
Billing UnitML
Marketing Start Date1996-06-01

NDC 0096-0709-60 [00096070960]

Xerac AC LIQUID
Marketing CategoryOTC monograph final
Application Numberpart350
Product TypeHUMAN OTC DRUG
Billing UnitML
Marketing Start Date1996-06-01

Drug Details

Active Ingredients

IngredientStrength
ALUMINUM CHLORIDE.0625 g/g

OpenFDA Data

SPL SET ID:59e37deb-01da-465f-b806-ff1a76255e71
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 197324

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