NDC 75197-006

Hands Wash-Free Disinfectant

Hands Wash-free Disinfectant

Hands Wash-Free Disinfectant is a Topical Gel in the Human Otc Drug category. It is labeled and distributed by Guangzhou Guangyi Biotechnology Co., Ltd.. The primary component is Alcohol.

Product ID75197-006_a379dbc5-5764-0e90-e053-2995a90a2786
NDC75197-006
Product TypeHuman Otc Drug
Proprietary NameHands Wash-Free Disinfectant
Generic NameHands Wash-free Disinfectant
Dosage FormGel
Route of AdministrationTOPICAL
Marketing Start Date2020-04-17
Marketing CategoryOTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL
Application Numberpart333A
Labeler NameGuangzhou Guangyi Biotechnology Co., Ltd.
Substance NameALCOHOL
Active Ingredient Strength70 mL/100mL
NDC Exclude FlagN
Listing Certified Through2021-12-31

Packaging

NDC 75197-006-03

60 mL in 1 BOTTLE (75197-006-03)
Marketing Start Date2020-04-17
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 75197-006-02 [75197000602]

Hands Wash-Free Disinfectant GEL
Marketing CategoryOTC monograph not final
Application Numberpart333A
Product TypeHUMAN OTC DRUG
Marketing Start Date2020-04-17

NDC 75197-006-03 [75197000603]

Hands Wash-Free Disinfectant GEL
Marketing CategoryOTC monograph not final
Application Numberpart333A
Product TypeHUMAN OTC DRUG
Marketing Start Date2020-04-17

NDC 75197-006-01 [75197000601]

Hands Wash-Free Disinfectant GEL
Marketing CategoryOTC monograph not final
Application Numberpart333A
Product TypeHUMAN OTC DRUG
Marketing Start Date2020-04-17

NDC 75197-006-06 [75197000606]

Hands Wash-Free Disinfectant GEL
Marketing CategoryOTC monograph not final
Application Numberpart333A
Product TypeHUMAN OTC DRUG
Marketing Start Date2020-04-17

NDC 75197-006-04 [75197000604]

Hands Wash-Free Disinfectant GEL
Marketing CategoryOTC monograph not final
Application Numberpart333A
Product TypeHUMAN OTC DRUG
Marketing Start Date2020-04-17

NDC 75197-006-05 [75197000605]

Hands Wash-Free Disinfectant GEL
Marketing CategoryOTC monograph not final
Application Numberpart333A
Product TypeHUMAN OTC DRUG
Marketing Start Date2020-04-17

Drug Details

Active Ingredients

IngredientStrength
ALCOHOL70 mL/100mL

OpenFDA Data

SPL SET ID:a379d7b2-cde9-d259-e053-2995a90aaa9f
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 581662
  • UPC Code
  • 6972523530538
  • 6972523530583
  • 6972523530521
  • 6972523530507
  • 6972523530286

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