NDC 75129-001

Hand Sanitizer (Rinse-free)

Hand Sanitizer (rinse-free)

Hand Sanitizer (Rinse-free) is a Topical Gel in the Human Otc Drug category. It is labeled and distributed by Shanghai Rayshine Envi-tech Developing Co., Ltd.. The primary component is Alcohol.

Product ID75129-001_a3886f94-1861-6910-e053-2995a90a1056
NDC75129-001
Product TypeHuman Otc Drug
Proprietary NameHand Sanitizer (Rinse-free)
Generic NameHand Sanitizer (rinse-free)
Dosage FormGel
Route of AdministrationTOPICAL
Marketing Start Date2020-04-18
Marketing CategoryOTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL
Application Numberpart333A
Labeler NameShanghai Rayshine ENVI-TECH Developing CO., Ltd.
Substance NameALCOHOL
Active Ingredient Strength62 mL/100mL
NDC Exclude FlagN
Listing Certified Through2021-12-31

Packaging

NDC 75129-001-01

30 mL in 1 BOTTLE (75129-001-01)
Marketing Start Date2020-04-18
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 75129-001-09 [75129000109]

Hand Sanitizer (Rinse-free) GEL
Marketing CategoryOTC monograph not final
Application Numberpart333A
Product TypeHUMAN OTC DRUG
Marketing Start Date2020-04-18

NDC 75129-001-12 [75129000112]

Hand Sanitizer (Rinse-free) GEL
Marketing CategoryOTC monograph not final
Application Numberpart333A
Product TypeHUMAN OTC DRUG
Marketing Start Date2020-04-18

NDC 75129-001-11 [75129000111]

Hand Sanitizer (Rinse-free) GEL
Marketing CategoryOTC monograph not final
Application Numberpart333A
Product TypeHUMAN OTC DRUG
Marketing Start Date2020-04-18

NDC 75129-001-01 [75129000101]

Hand Sanitizer (Rinse-free) GEL
Marketing CategoryOTC monograph not final
Application Numberpart333A
Product TypeHUMAN OTC DRUG
Marketing Start Date2020-04-18

NDC 75129-001-10 [75129000110]

Hand Sanitizer (Rinse-free) GEL
Marketing CategoryOTC monograph not final
Application Numberpart333A
Product TypeHUMAN OTC DRUG
Marketing Start Date2020-04-18

NDC 75129-001-13 [75129000113]

Hand Sanitizer (Rinse-free) GEL
Marketing CategoryOTC monograph not final
Application Numberpart333A
Product TypeHUMAN OTC DRUG
Marketing Start Date2020-04-18

NDC 75129-001-07 [75129000107]

Hand Sanitizer (Rinse-free) GEL
Marketing CategoryOTC monograph not final
Application Numberpart333A
Product TypeHUMAN OTC DRUG
Marketing Start Date2020-04-18

NDC 75129-001-08 [75129000108]

Hand Sanitizer (Rinse-free) GEL
Marketing CategoryOTC monograph not final
Application Numberpart333A
Product TypeHUMAN OTC DRUG
Marketing Start Date2020-04-18

NDC 75129-001-04 [75129000104]

Hand Sanitizer (Rinse-free) GEL
Marketing CategoryOTC monograph not final
Application Numberpart333A
Product TypeHUMAN OTC DRUG
Marketing Start Date2020-04-18

NDC 75129-001-02 [75129000102]

Hand Sanitizer (Rinse-free) GEL
Marketing CategoryOTC monograph not final
Application Numberpart333A
Product TypeHUMAN OTC DRUG
Marketing Start Date2020-04-18

NDC 75129-001-06 [75129000106]

Hand Sanitizer (Rinse-free) GEL
Marketing CategoryOTC monograph not final
Application Numberpart333A
Product TypeHUMAN OTC DRUG
Marketing Start Date2020-04-18

NDC 75129-001-03 [75129000103]

Hand Sanitizer (Rinse-free) GEL
Marketing CategoryOTC monograph not final
Application Numberpart333A
Product TypeHUMAN OTC DRUG
Marketing Start Date2020-04-18

NDC 75129-001-05 [75129000105]

Hand Sanitizer (Rinse-free) GEL
Marketing CategoryOTC monograph not final
Application Numberpart333A
Product TypeHUMAN OTC DRUG
Marketing Start Date2020-04-18

Drug Details

Active Ingredients

IngredientStrength
ALCOHOL62 mL/100mL

OpenFDA Data

SPL SET ID:a3886f94-1862-6910-e053-2995a90a1056
Manufacturer
UNII

NDC Crossover Matching brand name "Hand Sanitizer (Rinse-free)" or generic name "Hand Sanitizer (rinse-free)"

NDCBrand NameGeneric Name
75129-001Hand Sanitizer (Rinse-free)Hand Sanitizer (Rinse-free)
76700-001Hand Sanitizer (Rinse-free)Ethyl Alcohol
© 2025 FDA.report
This site is not affiliated with or endorsed by the FDA.