NDC 76881-005

Hand santiser

Hand Santiser

Hand santiser is a Topical Gel in the Human Otc Drug category. It is labeled and distributed by Yiwu City Jieyi Cleaning Supplies Co., Ltd. The primary component is Alcohol.

Product ID76881-005_a5a701d9-642e-88cf-e053-2a95a90a8a5f
NDC76881-005
Product TypeHuman Otc Drug
Proprietary NameHand santiser
Generic NameHand Santiser
Dosage FormGel
Route of AdministrationTOPICAL
Marketing Start Date2020-03-30
Marketing CategoryOTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL
Application Numberpart333A
Labeler NameYiwu city jieyi cleaning supplies co., LTD
Substance NameALCOHOL
Active Ingredient Strength75 mL/100mL
NDC Exclude FlagN
Listing Certified Through2021-12-31

Packaging

NDC 76881-005-01

30 mL in 1 BOTTLE (76881-005-01)
Marketing Start Date2020-03-30
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 76881-005-02 [76881000502]

Hand santiser GEL
Marketing CategoryOTC monograph not final
Application Numberpart333A
Product TypeHUMAN OTC DRUG
Marketing Start Date2020-03-30

NDC 76881-005-04 [76881000504]

Hand santiser GEL
Marketing CategoryOTC monograph not final
Application Numberpart333A
Product TypeHUMAN OTC DRUG
Marketing Start Date2020-03-30

NDC 76881-005-07 [76881000507]

Hand santiser GEL
Marketing CategoryOTC monograph not final
Application Numberpart333A
Product TypeHUMAN OTC DRUG
Marketing Start Date2020-03-30

NDC 76881-005-05 [76881000505]

Hand santiser GEL
Marketing CategoryOTC monograph not final
Application Numberpart333A
Product TypeHUMAN OTC DRUG
Marketing Start Date2020-03-30

NDC 76881-005-03 [76881000503]

Hand santiser GEL
Marketing CategoryOTC monograph not final
Application Numberpart333A
Product TypeHUMAN OTC DRUG
Marketing Start Date2020-03-30

NDC 76881-005-06 [76881000506]

Hand santiser GEL
Marketing CategoryOTC monograph not final
Application Numberpart333A
Product TypeHUMAN OTC DRUG
Marketing Start Date2020-03-30

NDC 76881-005-01 [76881000501]

Hand santiser GEL
Marketing CategoryOTC monograph not final
Application Numberpart333A
Product TypeHUMAN OTC DRUG
Marketing Start Date2020-03-30

Drug Details


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