NDC 61357-152

Sanafitil Talco

Undecylenic Acid And Zinc Undecylenate

Sanafitil Talco is a Topical Powder in the Human Otc Drug category. It is labeled and distributed by Zurich Medical Labs, Llc. The primary component is Undecylenic Acid; Zinc Undecylenate.

Product ID61357-152_4b57c6de-c555-41a0-8789-4cc84a62f16b
NDC61357-152
Product TypeHuman Otc Drug
Proprietary NameSanafitil Talco
Generic NameUndecylenic Acid And Zinc Undecylenate
Dosage FormPowder
Route of AdministrationTOPICAL
Marketing Start Date1966-08-24
Marketing CategoryOTC MONOGRAPH FINAL / OTC MONOGRAPH FINAL
Application Numberpart333C
Labeler NameZURICH MEDICAL LABS, LLC
Substance NameUNDECYLENIC ACID; ZINC UNDECYLENATE
Active Ingredient Strength20 mg/g; mg/g
NDC Exclude FlagE
Listing Certified Through2017-12-31

Packaging

NDC 61357-152-01

1 BOTTLE in 1 CARTON (61357-152-01) > 57 g in 1 BOTTLE
Marketing Start Date1966-08-24
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 61357-152-01 [61357015201]

Sanafitil Talco POWDER
Marketing CategoryOTC MONOGRAPH FINAL
Application Numberpart333C
Product TypeHUMAN OTC DRUG
Marketing Start Date1966-08-24
Inactivation Date2019-11-27

Drug Details

Active Ingredients

IngredientStrength
UNDECYLENIC ACID20 mg/g

OpenFDA Data

SPL SET ID:105c961c-81ee-4b44-b39e-1501132114f0
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 1491970
  • 313817

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