NDC 63533-221

Han-I-Size

Alcohol

Han-I-Size is a Topical Gel in the Human Otc Drug category. It is labeled and distributed by Momar Incorporated. The primary component is Alcohol.

Product ID63533-221_2d0de76a-fd02-4900-8f0c-335e1d9af17b
NDC63533-221
Product TypeHuman Otc Drug
Proprietary NameHan-I-Size
Generic NameAlcohol
Dosage FormGel
Route of AdministrationTOPICAL
Marketing Start Date2005-12-01
Marketing CategoryOTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL
Application Numberpart333E
Labeler NameMomar Incorporated
Substance NameALCOHOL
Active Ingredient Strength1 mL/mL
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 63533-221-14

3785 mL in 1 BOTTLE, PLASTIC (63533-221-14)
Marketing Start Date2005-12-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 63533-221-10 [63533022110]

Han-I-Size GEL
Marketing CategoryOTC monograph not final
Application Numberpart333E
Product TypeHUMAN OTC DRUG
Marketing Start Date2005-12-01
Marketing End Date2018-12-05

NDC 63533-221-15 [63533022115]

Han-I-Size GEL
Marketing CategoryOTC monograph not final
Application Numberpart333E
Product TypeHUMAN OTC DRUG
Marketing Start Date2005-12-01
Marketing End Date2018-12-05

NDC 63533-221-14 [63533022114]

Han-I-Size GEL
Marketing CategoryOTC monograph not final
Application Numberpart333E
Product TypeHUMAN OTC DRUG
Marketing Start Date2005-12-01

NDC 63533-221-55 [63533022155]

Han-I-Size GEL
Marketing CategoryOTC monograph not final
Application Numberpart333E
Product TypeHUMAN OTC DRUG
Marketing Start Date2005-12-01
Marketing End Date2018-12-05

NDC 63533-221-11 [63533022111]

Han-I-Size GEL
Marketing CategoryOTC monograph not final
Application Numberpart333E
Product TypeHUMAN OTC DRUG
Marketing Start Date2005-12-01
Marketing End Date2018-12-05

NDC 63533-221-09 [63533022109]

Han-I-Size GEL
Marketing CategoryOTC monograph not final
Application Numberpart333E
Product TypeHUMAN OTC DRUG
Marketing Start Date2005-12-01
Marketing End Date2018-12-05

NDC 63533-221-03 [63533022103]

Han-I-Size GEL
Marketing CategoryOTC monograph not final
Application Numberpart333E
Product TypeHUMAN OTC DRUG
Marketing Start Date2005-12-01
Marketing End Date2018-12-05

NDC 63533-221-05 [63533022105]

Han-I-Size GEL
Marketing CategoryOTC monograph not final
Application Numberpart333E
Product TypeHUMAN OTC DRUG
Marketing Start Date2005-12-01
Marketing End Date2018-12-05

NDC 63533-221-08 [63533022108]

Han-I-Size GEL
Marketing CategoryOTC monograph not final
Application Numberpart333E
Product TypeHUMAN OTC DRUG
Marketing Start Date2005-12-01
Marketing End Date2018-12-05

NDC 63533-221-24 [63533022124]

Han-I-Size GEL
Marketing CategoryOTC monograph not final
Application Numberpart333E
Product TypeHUMAN OTC DRUG
Marketing Start Date2005-12-01
Marketing End Date2018-12-05

NDC 63533-221-17 [63533022117]

Han-I-Size GEL
Marketing CategoryOTC monograph not final
Application Numberpart333E
Product TypeHUMAN OTC DRUG
Marketing Start Date2005-12-01
Marketing End Date2018-12-05

NDC 63533-221-01 [63533022101]

Han-I-Size GEL
Marketing CategoryOTC monograph not final
Application Numberpart333E
Product TypeHUMAN OTC DRUG
Marketing Start Date2005-12-01
Marketing End Date2018-12-05

NDC 63533-221-12 [63533022112]

Han-I-Size GEL
Marketing CategoryOTC monograph not final
Application Numberpart333E
Product TypeHUMAN OTC DRUG
Marketing Start Date2005-12-01
Marketing End Date2018-12-05

NDC 63533-221-07 [63533022107]

Han-I-Size GEL
Marketing CategoryOTC monograph not final
Application Numberpart333E
Product TypeHUMAN OTC DRUG
Marketing Start Date2005-12-01
Marketing End Date2018-12-05

NDC 63533-221-28 [63533022128]

Han-I-Size GEL
Marketing CategoryOTC monograph not final
Application Numberpart333E
Product TypeHUMAN OTC DRUG
Marketing Start Date2005-12-01

NDC 63533-221-13 [63533022113]

Han-I-Size GEL
Marketing CategoryOTC monograph not final
Application Numberpart333E
Product TypeHUMAN OTC DRUG
Marketing Start Date2005-12-01
Marketing End Date2018-12-05

NDC 63533-221-27 [63533022127]

Han-I-Size GEL
Marketing CategoryOTC monograph not final
Application Numberpart333E
Product TypeHUMAN OTC DRUG
Marketing Start Date2005-12-01
Marketing End Date2018-12-05

NDC 63533-221-06 [63533022106]

Han-I-Size GEL
Marketing CategoryOTC monograph not final
Application Numberpart333E
Product TypeHUMAN OTC DRUG
Marketing Start Date2005-12-01
Marketing End Date2018-12-05

Drug Details

Active Ingredients

IngredientStrength
ALCOHOL.7 mL/mL

OpenFDA Data

SPL SET ID:3817bf34-c8fc-4dfe-a29f-14ba15ef11ed
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 581662
  • NDC Crossover Matching brand name "Han-I-Size" or generic name "Alcohol"

    NDCBrand NameGeneric Name
    63533-221Han-I-SizeHan-I-Size
    63533-001HAN-I-SIZEHAN-I-SIZE
    0363-0370Advanced Hand SanitizerAlcohol
    0363-9776Advanced Hand SanitizerAlcohol
    0363-0046AlcoholAlcohol
    0074-9857Alcohol - Hand SanitizerAlcohol
    0065-8000Alcohol Antiseptic 80%Alcohol
    0404-0122Antibacterialalcohol
    0395-0040Ethyl Rubbing AlcoholAlcohol
    0363-0968Hand SanitizerALCOHOL
    0219-2020Humphreys Alcoholado MaravillaALCOHOL
    0404-5988Instant Hand Sanitizeralcohol
    0295-9025Nozin Nasal SanitizerAlcohol
    0362-6000SeptoSanAlcohol
    0362-6001SeptoSanAlcohol
    0362-6002SeptoSanAlcohol
    0064-1050TRISEPTINALCOHOL
    0363-1305WalgreensAlcohol
    0363-1306WalgreensAlcohol
    0363-1307WalgreensAlcohol
    0363-1308WalgreensAlcohol
    0363-1309WalgreensAlcohol
    0363-0969Walgreens Advanced Hand Sanitizer Citrus ScentAlcohol
    0363-9005Walgreens Advanced Hand Sanitizer Made with Plant-Based Ethyl AlcoholAlcohol
    0363-9003Walgreens Advanced Hand Sanitizer with Aloe and Vitamin EAlcohol
    0363-0967WALGREENS ADVANCED HAND SANITIZER WITH FRESH SCENTALCOHOL
    0363-9004Walgreens Advanced Hand Sanitizer with Vitamin EAlcohol
    0363-9008Walgreens Advanced Hand Sanitizer with Vitamin EAlcohol
    0363-9006Walgreens Hand Sanitizer Coastal Breeze ScentAlcohol
    0363-9007Walgreens Hand Sanitizer Crisp Apple ScentAlcohol

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