NDC 74279-0008

Wonder Hand Gel (Ethanol)

Alcohol

Wonder Hand Gel (Ethanol) is a Topical Liquid in the Human Otc Drug category. It is labeled and distributed by Dai Kyoung Pharmaceutic Co.,ltd.. The primary component is Alcohol.

Product ID74279-0008_a50e1309-9ee7-f5ef-e053-2995a90a6e89
NDC74279-0008
Product TypeHuman Otc Drug
Proprietary NameWonder Hand Gel (Ethanol)
Generic NameAlcohol
Dosage FormLiquid
Route of AdministrationTOPICAL
Marketing Start Date2020-04-10
Marketing CategoryOTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL
Application Numberpart333A
Labeler NameDai Kyoung Pharmaceutic Co.,Ltd.
Substance NameALCOHOL
Active Ingredient Strength540 mL/750mL
NDC Exclude FlagN
Listing Certified Through2021-12-31

Packaging

NDC 74279-0008-1

750 mL in 1 BOTTLE, PUMP (74279-0008-1)
Marketing Start Date2020-04-10
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 74279-0008-1 [74279000801]

Wonder Hand Gel (Ethanol) LIQUID
Marketing CategoryOTC monograph not final
Application Numberpart333A
Product TypeHUMAN OTC DRUG
Marketing Start Date2020-04-10
Marketing End Date2020-05-11

Drug Details

Active Ingredients

IngredientStrength
ALCOHOL540 mL/750mL

NDC Crossover Matching brand name "Wonder Hand Gel (Ethanol)" or generic name "Alcohol"

NDCBrand NameGeneric Name
74279-0001Wonder Hand Gel (Ethanol)Wonder Hand Gel (Ethanol)
74279-0007Wonder Hand Gel (Ethanol)Wonder Hand Gel (Ethanol)
74279-0008Wonder Hand Gel (Ethanol)Wonder Hand Gel (Ethanol)
74279-0009Wonder Hand Gel (Ethanol)Wonder Hand Gel (Ethanol)
74279-0010Wonder Hand Gel (Ethanol)Wonder Hand Gel (Ethanol)
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0363-1306WalgreensAlcohol
0363-1307WalgreensAlcohol
0363-1308WalgreensAlcohol
0363-1309WalgreensAlcohol
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