NDC 75212-001

ANTIBACTERIAL HANDS-FREE Gel

Antibacterial Hands-free Gel

ANTIBACTERIAL HANDS-FREE Gel is a Topical Gel in the Human Otc Drug category. It is labeled and distributed by Guangzhou Yuncai Fine Chemical Co.ltd. The primary component is Alcohol.

Product ID75212-001_a352d03c-396a-cb4b-e053-2a95a90a24c5
NDC75212-001
Product TypeHuman Otc Drug
Proprietary NameANTIBACTERIAL HANDS-FREE Gel
Generic NameAntibacterial Hands-free Gel
Dosage FormGel
Route of AdministrationTOPICAL
Marketing Start Date2020-04-15
Marketing CategoryOTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL
Application Numberpart333A
Labeler NameGuangzhou Yuncai Fine Chemical CO.LTD
Substance NameALCOHOL
Active Ingredient Strength75 mL/100mL
NDC Exclude FlagN
Listing Certified Through2021-12-31

Packaging

NDC 75212-001-01

50 mL in 1 BOTTLE (75212-001-01)
Marketing Start Date2020-04-15
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 75212-001-04 [75212000104]

ANTIBACTERIAL HANDS-FREE Gel GEL
Marketing CategoryOTC monograph not final
Application Numberpart333A
Product TypeHUMAN OTC DRUG
Marketing Start Date2020-04-15

NDC 75212-001-06 [75212000106]

ANTIBACTERIAL HANDS-FREE Gel GEL
Marketing CategoryOTC monograph not final
Application Numberpart333A
Product TypeHUMAN OTC DRUG
Marketing Start Date2020-04-15

NDC 75212-001-02 [75212000102]

ANTIBACTERIAL HANDS-FREE Gel GEL
Marketing CategoryOTC monograph not final
Application Numberpart333A
Product TypeHUMAN OTC DRUG
Marketing Start Date2020-04-15

NDC 75212-001-03 [75212000103]

ANTIBACTERIAL HANDS-FREE Gel GEL
Marketing CategoryOTC monograph not final
Application Numberpart333A
Product TypeHUMAN OTC DRUG
Marketing Start Date2020-04-15

NDC 75212-001-01 [75212000101]

ANTIBACTERIAL HANDS-FREE Gel GEL
Marketing CategoryOTC monograph not final
Application Numberpart333A
Product TypeHUMAN OTC DRUG
Marketing Start Date2020-04-15

NDC 75212-001-05 [75212000105]

ANTIBACTERIAL HANDS-FREE Gel GEL
Marketing CategoryOTC monograph not final
Application Numberpart333A
Product TypeHUMAN OTC DRUG
Marketing Start Date2020-04-15

Drug Details

Active Ingredients

IngredientStrength
ALCOHOL75 mL/100mL

OpenFDA Data

SPL SET ID:a352d09c-ee41-b009-e053-2a95a90a3940
Manufacturer
UNII
UPC Code
  • 6935985115019

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