NDC 74010-3016

Hand Sanitizer USA

Hand Sanitizer Usa

Hand Sanitizer USA is a Topical Liquid in the Human Otc Drug category. It is labeled and distributed by Global Universal Srl Llc Dba Minhas Micro Distillery. The primary component is Alcohol.

Product ID74010-3016_a1c461af-5f24-085c-e053-2995a90a12da
NDC74010-3016
Product TypeHuman Otc Drug
Proprietary NameHand Sanitizer USA
Generic NameHand Sanitizer Usa
Dosage FormLiquid
Route of AdministrationTOPICAL
Marketing Start Date2020-03-26
Marketing CategoryOTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL
Application Numberpart333A
Labeler NameGlobal Universal SRL LLC dba Minhas Micro Distillery
Substance NameALCOHOL
Active Ingredient Strength80 mL/100mL
NDC Exclude FlagN
Listing Certified Through2021-12-31

Packaging

NDC 74010-3016-1

50 mL in 1 BOTTLE, PLASTIC (74010-3016-1)
Marketing Start Date2020-03-30
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 74010-3016-6 [74010301606]

Hand Sanitizer USA LIQUID
Marketing CategoryOTC monograph not final
Application Numberpart333A
Product TypeHUMAN OTC DRUG
Marketing Start Date2020-03-30

NDC 74010-3016-4 [74010301604]

Hand Sanitizer USA LIQUID
Marketing CategoryOTC monograph not final
Application Numberpart333A
Product TypeHUMAN OTC DRUG
Marketing Start Date2020-03-30

NDC 74010-3016-2 [74010301602]

Hand Sanitizer USA LIQUID
Marketing CategoryOTC monograph not final
Application Numberpart333A
Product TypeHUMAN OTC DRUG
Marketing Start Date2020-03-30

NDC 74010-3016-5 [74010301605]

Hand Sanitizer USA LIQUID
Marketing CategoryOTC monograph not final
Application Numberpart333A
Product TypeHUMAN OTC DRUG
Marketing Start Date2020-03-30

NDC 74010-3016-3 [74010301603]

Hand Sanitizer USA LIQUID
Marketing CategoryOTC monograph not final
Application Numberpart333A
Product TypeHUMAN OTC DRUG
Marketing Start Date2020-03-30

NDC 74010-3016-1 [74010301601]

Hand Sanitizer USA LIQUID
Marketing CategoryOTC monograph not final
Application Numberpart333A
Product TypeHUMAN OTC DRUG
Marketing Start Date2020-03-30

Drug Details

Active Ingredients

IngredientStrength
ALCOHOL80 mL/100mL

OpenFDA Data

SPL SET ID:a1c461af-5f23-085c-e053-2995a90a12da
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 1039339
  • UPC Code
  • 0085254130147
  • 0085254130109
  • 0085254130154
  • 0085254130178
  • 0085254130123
  • 0085254130130
  • 0085254130116

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