NDC 74563-001

Mr Toms Hand Sanitizer

Mr Toms Hand Sanitizer

Mr Toms Hand Sanitizer is a Topical Liquid in the Human Otc Drug category. It is labeled and distributed by List Distillery, Llc. The primary component is Alcohol.

Product ID74563-001_a2621c15-1058-12cb-e053-2a95a90abab0
NDC74563-001
Product TypeHuman Otc Drug
Proprietary NameMr Toms Hand Sanitizer
Generic NameMr Toms Hand Sanitizer
Dosage FormLiquid
Route of AdministrationTOPICAL
Marketing Start Date2020-04-03
Marketing CategoryOTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL
Application Numberpart333A
Labeler NameList Distillery, LLC
Substance NameALCOHOL
Active Ingredient Strength800 mL/1000mL
NDC Exclude FlagN
Listing Certified Through2021-12-31

Packaging

NDC 74563-001-03

1895 mL in 1 BOTTLE, PLASTIC (74563-001-03)
Marketing Start Date2020-04-03
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 74563-001-01 [74563000101]

Mr Toms Hand Sanitizer LIQUID
Marketing CategoryOTC monograph not final
Application Numberpart333A
Product TypeHUMAN OTC DRUG
Marketing Start Date2020-04-03

NDC 74563-001-06 [74563000106]

Mr Toms Hand Sanitizer LIQUID
Marketing CategoryOTC monograph not final
Application Numberpart333A
Product TypeHUMAN OTC DRUG
Marketing Start Date2020-04-03

NDC 74563-001-05 [74563000105]

Mr Toms Hand Sanitizer LIQUID
Marketing CategoryOTC monograph not final
Application Numberpart333A
Product TypeHUMAN OTC DRUG
Marketing Start Date2020-04-03

NDC 74563-001-03 [74563000103]

Mr Toms Hand Sanitizer LIQUID
Marketing CategoryOTC monograph not final
Application Numberpart333A
Product TypeHUMAN OTC DRUG
Marketing Start Date2020-04-03

NDC 74563-001-04 [74563000104]

Mr Toms Hand Sanitizer LIQUID
Marketing CategoryOTC monograph not final
Application Numberpart333A
Product TypeHUMAN OTC DRUG
Marketing Start Date2020-04-03

NDC 74563-001-02 [74563000102]

Mr Toms Hand Sanitizer LIQUID
Marketing CategoryOTC monograph not final
Application Numberpart333A
Product TypeHUMAN OTC DRUG
Marketing Start Date2020-04-03

Drug Details

Active Ingredients

IngredientStrength
ALCOHOL800 mL/1000mL

OpenFDA Data

SPL SET ID:a2621c15-1057-12cb-e053-2a95a90abab0
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 1039339

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