NDC 74760-001

REPAND ANTIBACTERIAL HAND SANITIZER

Repand Antibacterial Hand Sanitizer

REPAND ANTIBACTERIAL HAND SANITIZER is a Topical Gel in the Human Otc Drug category. It is labeled and distributed by Guangzhou Gaozi Cosmetics Co., Ltd. The primary component is Alcohol.

Product ID74760-001_a2114df4-99c7-9833-e053-2a95a90aaa29
NDC74760-001
Product TypeHuman Otc Drug
Proprietary NameREPAND ANTIBACTERIAL HAND SANITIZER
Generic NameRepand Antibacterial Hand Sanitizer
Dosage FormGel
Route of AdministrationTOPICAL
Marketing Start Date2020-04-23
Marketing CategoryOTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL
Application Numberpart333A
Labeler NameGUANGZHOU GAOZI COSMETICS CO., LTD
Substance NameALCOHOL
Active Ingredient Strength70 mL/100mL
NDC Exclude FlagN
Listing Certified Through2021-12-31

Packaging

NDC 74760-001-01

60 mL in 1 BOTTLE (74760-001-01)
Marketing Start Date2020-04-23
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 74760-001-03 [74760000103]

REPAND ANTIBACTERIAL HAND SANITIZER GEL
Marketing CategoryOTC monograph not final
Application Numberpart333A
Product TypeHUMAN OTC DRUG
Marketing Start Date2020-04-23

NDC 74760-001-05 [74760000105]

REPAND ANTIBACTERIAL HAND SANITIZER GEL
Marketing CategoryOTC monograph not final
Application Numberpart333A
Product TypeHUMAN OTC DRUG
Marketing Start Date2020-04-23

NDC 74760-001-04 [74760000104]

REPAND ANTIBACTERIAL HAND SANITIZER GEL
Marketing CategoryOTC monograph not final
Application Numberpart333A
Product TypeHUMAN OTC DRUG
Marketing Start Date2020-04-23

NDC 74760-001-02 [74760000102]

REPAND ANTIBACTERIAL HAND SANITIZER GEL
Marketing CategoryOTC monograph not final
Application Numberpart333A
Product TypeHUMAN OTC DRUG
Marketing Start Date2020-04-23

NDC 74760-001-06 [74760000106]

REPAND ANTIBACTERIAL HAND SANITIZER GEL
Marketing CategoryOTC monograph not final
Application Numberpart333A
Product TypeHUMAN OTC DRUG
Marketing Start Date2020-04-23

NDC 74760-001-01 [74760000101]

REPAND ANTIBACTERIAL HAND SANITIZER GEL
Marketing CategoryOTC monograph not final
Application Numberpart333A
Product TypeHUMAN OTC DRUG
Marketing Start Date2020-04-23

Drug Details

Active Ingredients

IngredientStrength
ALCOHOL70 mL/100mL

OpenFDA Data

SPL SET ID:a3f0354d-8c7d-1ec2-e053-2995a90add52
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 581662
  • UPC Code
  • 6927382642298
  • 6927382642243

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