NDC 74881-001

DISINFECTION HAND SANITIZER GEl

Disinfection Hand Sanitizer Gel

DISINFECTION HAND SANITIZER GEl is a Topical Gel in the Human Otc Drug category. It is labeled and distributed by Huizhou Baozi Biotechnology Co., Ltd.. The primary component is Alcohol.

Product ID74881-001_a2c35647-40f3-5ef5-e053-2a95a90a9da0
NDC74881-001
Product TypeHuman Otc Drug
Proprietary NameDISINFECTION HAND SANITIZER GEl
Generic NameDisinfection Hand Sanitizer Gel
Dosage FormGel
Route of AdministrationTOPICAL
Marketing Start Date2020-04-08
Marketing CategoryOTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL
Application Numberpart333A
Labeler NameHuizhou Baozi Biotechnology Co., Ltd.
Substance NameALCOHOL
Active Ingredient Strength75 mL/100mL
NDC Exclude FlagN
Listing Certified Through2021-12-31

Packaging

NDC 74881-001-01

500 mL in 1 BOTTLE (74881-001-01)
Marketing Start Date2020-04-08
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 74881-001-04 [74881000104]

DISINFECTION HAND SANITIZER GEl GEL
Marketing CategoryOTC monograph not final
Application Numberpart333A
Product TypeHUMAN OTC DRUG
Marketing Start Date2020-04-08

NDC 74881-001-08 [74881000108]

DISINFECTION HAND SANITIZER GEl GEL
Marketing CategoryOTC monograph not final
Application Numberpart333A
Product TypeHUMAN OTC DRUG
Marketing Start Date2020-04-08

NDC 74881-001-13 [74881000113]

DISINFECTION HAND SANITIZER GEl GEL
Marketing CategoryOTC monograph not final
Application Numberpart333A
Product TypeHUMAN OTC DRUG
Marketing Start Date2020-04-08

NDC 74881-001-11 [74881000111]

DISINFECTION HAND SANITIZER GEl GEL
Marketing CategoryOTC monograph not final
Application Numberpart333A
Product TypeHUMAN OTC DRUG
Marketing Start Date2020-04-08

NDC 74881-001-07 [74881000107]

DISINFECTION HAND SANITIZER GEl GEL
Marketing CategoryOTC monograph not final
Application Numberpart333A
Product TypeHUMAN OTC DRUG
Marketing Start Date2020-04-08

NDC 74881-001-15 [74881000115]

DISINFECTION HAND SANITIZER GEl GEL
Marketing CategoryOTC monograph not final
Application Numberpart333A
Product TypeHUMAN OTC DRUG
Marketing Start Date2020-04-08

NDC 74881-001-16 [74881000116]

DISINFECTION HAND SANITIZER GEl GEL
Marketing CategoryOTC monograph not final
Application Numberpart333A
Product TypeHUMAN OTC DRUG
Marketing Start Date2020-04-08

NDC 74881-001-02 [74881000102]

DISINFECTION HAND SANITIZER GEl GEL
Marketing CategoryOTC monograph not final
Application Numberpart333A
Product TypeHUMAN OTC DRUG
Marketing Start Date2020-04-08

NDC 74881-001-12 [74881000112]

DISINFECTION HAND SANITIZER GEl GEL
Marketing CategoryOTC monograph not final
Application Numberpart333A
Product TypeHUMAN OTC DRUG
Marketing Start Date2020-04-08

NDC 74881-001-03 [74881000103]

DISINFECTION HAND SANITIZER GEl GEL
Marketing CategoryOTC monograph not final
Application Numberpart333A
Product TypeHUMAN OTC DRUG
Marketing Start Date2020-04-08

NDC 74881-001-06 [74881000106]

DISINFECTION HAND SANITIZER GEl GEL
Marketing CategoryOTC monograph not final
Application Numberpart333A
Product TypeHUMAN OTC DRUG
Marketing Start Date2020-04-08

NDC 74881-001-05 [74881000105]

DISINFECTION HAND SANITIZER GEl GEL
Marketing CategoryOTC monograph not final
Application Numberpart333A
Product TypeHUMAN OTC DRUG
Marketing Start Date2020-04-08

NDC 74881-001-10 [74881000110]

DISINFECTION HAND SANITIZER GEl GEL
Marketing CategoryOTC monograph not final
Application Numberpart333A
Product TypeHUMAN OTC DRUG
Marketing Start Date2020-04-08

NDC 74881-001-01 [74881000101]

DISINFECTION HAND SANITIZER GEl GEL
Marketing CategoryOTC monograph not final
Application Numberpart333A
Product TypeHUMAN OTC DRUG
Marketing Start Date2020-04-08

NDC 74881-001-09 [74881000109]

DISINFECTION HAND SANITIZER GEl GEL
Marketing CategoryOTC monograph not final
Application Numberpart333A
Product TypeHUMAN OTC DRUG
Marketing Start Date2020-04-08

NDC 74881-001-14 [74881000114]

DISINFECTION HAND SANITIZER GEl GEL
Marketing CategoryOTC monograph not final
Application Numberpart333A
Product TypeHUMAN OTC DRUG
Marketing Start Date2020-04-08

Drug Details

Active Ingredients

IngredientStrength
ALCOHOL75 mL/100mL

OpenFDA Data

SPL SET ID:a2c35647-40f5-5ef5-e053-2a95a90a9da0
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 1305100
  • UPC Code
  • 6970715016860
  • 6971555291141

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