NDC 70108-021

Minions Hand Sanitizer

Ethyl Alcohol

Minions Hand Sanitizer is a Topical Liquid in the Human Otc Drug category. It is labeled and distributed by Ashtel Studios, Inc.. The primary component is Alcohol.

Product ID70108-021_673dc2b5-4177-43b8-b38a-9e3fd7454886
NDC70108-021
Product TypeHuman Otc Drug
Proprietary NameMinions Hand Sanitizer
Generic NameEthyl Alcohol
Dosage FormLiquid
Route of AdministrationTOPICAL
Marketing Start Date2019-10-24
Marketing CategoryOTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL
Application Numberpart333A
Labeler NameAshtel Studios, Inc.
Substance NameALCOHOL
Active Ingredient Strength62 mL/100mL
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 70108-021-01

53 mL in 1 BOTTLE (70108-021-01)
Marketing Start Date2019-10-24
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 70108-021-01 [70108002101]

Minions Hand Sanitizer LIQUID
Marketing CategoryOTC monograph not final
Application Numberpart333A
Product TypeHUMAN OTC DRUG
Marketing Start Date2019-10-24

Drug Details

Active Ingredients

IngredientStrength
ALCOHOL62 mL/100mL

NDC Crossover Matching brand name "Minions Hand Sanitizer" or generic name "Ethyl Alcohol"

NDCBrand NameGeneric Name
70108-021Minions Hand SanitizerMinions Hand Sanitizer
70108-023Minions Hand SanitizerMinions Hand Sanitizer
0363-1050A Little Something Eucalyptus Mist Hand SanitierEthyl Alcohol
0363-1051A Little Something Prosecco Bubbles Hand SanitizerEthyl Alcohol
0363-0952Advanced Hand SanitizerEthyl Alcohol
0363-0663Crisp Apple Hand SaniEthyl Alcohol
0363-0876Ethyl Rubbing AlcoholEthyl Alcohol
0113-7077hand sanitizerethyl alcohol
0363-0469Hand SanitizerEthyl Alcohol
0363-0596Hand SanitizerEthyl Alcohol
0363-0643Hand SanitizerEthyl Alcohol
0363-0826Hand SanitizerEthyl Alcohol
0363-0890Hand SanitizerEthyl Alcohol
0363-0898Hand SanitizerEthyl Alcohol
0363-0984Hand SanitizerEthyl Alcohol
0064-1080SURGICEPTethyl alcohol
0363-5721WalgreensEthyl Alcohol

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.