NDC 63533-585

Han-I-Foam

Alcohol

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

Product ID63533-585_8260614a-0d0d-4f14-bbf2-7a5da5d77feb
NDC63533-585
Product TypeHuman Otc Drug
Proprietary NameHan-I-Foam
Generic NameAlcohol
Dosage FormLiquid
Route of AdministrationTOPICAL
Marketing Start Date2009-09-01
Marketing CategoryOTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL
Application Numberpart333
Labeler NameMomar Incorporated
Substance NameALCOHOL
Active Ingredient Strength1 mL/mL
NDC Exclude FlagE
Listing Certified Through2018-12-31

Packaging

NDC 63533-585-55

208200 mL in 1 DRUM (63533-585-55)
Marketing Start Date2009-09-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 63533-585-06 [63533058506]

Han-I-Foam LIQUID
Marketing CategoryOTC monograph not final
Application Numberpart333
Product TypeHUMAN OTC DRUG
Marketing Start Date2009-09-01
Inactivation Date2020-01-31

NDC 63533-585-13 [63533058513]

Han-I-Foam LIQUID
Marketing CategoryOTC monograph not final
Application Numberpart333
Product TypeHUMAN OTC DRUG
Marketing Start Date2009-09-01
Inactivation Date2020-01-31

NDC 63533-585-11 [63533058511]

Han-I-Foam LIQUID
Marketing CategoryOTC monograph not final
Application Numberpart333
Product TypeHUMAN OTC DRUG
Marketing Start Date2009-09-01
Inactivation Date2020-01-31

NDC 63533-585-05 [63533058505]

Han-I-Foam LIQUID
Marketing CategoryOTC monograph not final
Application Numberpart333
Product TypeHUMAN OTC DRUG
Marketing Start Date2009-09-01
Inactivation Date2020-01-31

NDC 63533-585-24 [63533058524]

Han-I-Foam LIQUID
Marketing CategoryOTC monograph not final
Application Numberpart333
Product TypeHUMAN OTC DRUG
Marketing Start Date2009-09-01
Inactivation Date2020-01-31

NDC 63533-585-08 [63533058508]

Han-I-Foam LIQUID
Marketing CategoryOTC monograph not final
Application Numberpart333
Product TypeHUMAN OTC DRUG
Marketing Start Date2009-09-01
Inactivation Date2020-01-31

NDC 63533-585-07 [63533058507]

Han-I-Foam LIQUID
Marketing CategoryOTC monograph not final
Application Numberpart333
Product TypeHUMAN OTC DRUG
Marketing Start Date2009-09-01
Inactivation Date2020-01-31

NDC 63533-585-10 [63533058510]

Han-I-Foam LIQUID
Marketing CategoryOTC monograph not final
Application Numberpart333
Product TypeHUMAN OTC DRUG
Marketing Start Date2009-09-01
Inactivation Date2020-01-31

NDC 63533-585-16 [63533058516]

Han-I-Foam LIQUID
Marketing CategoryOTC monograph not final
Application Numberpart333
Product TypeHUMAN OTC DRUG
Marketing Start Date2009-09-01
Inactivation Date2020-01-31

NDC 63533-585-01 [63533058501]

Han-I-Foam LIQUID
Marketing CategoryOTC monograph not final
Application Numberpart333
Product TypeHUMAN OTC DRUG
Marketing Start Date2009-09-01
Inactivation Date2020-01-31

NDC 63533-585-55 [63533058555]

Han-I-Foam LIQUID
Marketing CategoryOTC monograph not final
Application Numberpart333
Product TypeHUMAN OTC DRUG
Marketing Start Date2009-09-01
Inactivation Date2020-01-31

NDC 63533-585-28 [63533058528]

Han-I-Foam LIQUID
Marketing CategoryOTC monograph not final
Application Numberpart333
Product TypeHUMAN OTC DRUG
Marketing Start Date2009-09-01
Inactivation Date2020-01-31

NDC 63533-585-03 [63533058503]

Han-I-Foam LIQUID
Marketing CategoryOTC monograph not final
Application Numberpart333
Product TypeHUMAN OTC DRUG
Marketing Start Date2009-09-01
Inactivation Date2020-01-31

NDC 63533-585-12 [63533058512]

Han-I-Foam LIQUID
Marketing CategoryOTC monograph not final
Application Numberpart333
Product TypeHUMAN OTC DRUG
Marketing Start Date2009-09-01
Inactivation Date2020-01-31

NDC 63533-585-17 [63533058517]

Han-I-Foam LIQUID
Marketing CategoryOTC monograph not final
Application Numberpart333
Product TypeHUMAN OTC DRUG
Marketing Start Date2009-09-01
Inactivation Date2020-01-31

NDC 63533-585-15 [63533058515]

Han-I-Foam LIQUID
Marketing CategoryOTC monograph not final
Application Numberpart333
Product TypeHUMAN OTC DRUG
Marketing Start Date2009-09-01
Inactivation Date2020-01-31

NDC 63533-585-27 [63533058527]

Han-I-Foam LIQUID
Marketing CategoryOTC monograph not final
Application Numberpart333
Product TypeHUMAN OTC DRUG
Marketing Start Date2009-09-01
Inactivation Date2020-01-31

NDC 63533-585-09 [63533058509]

Han-I-Foam LIQUID
Marketing CategoryOTC monograph not final
Application Numberpart333
Product TypeHUMAN OTC DRUG
Marketing Start Date2009-09-01
Inactivation Date2020-01-31

NDC 63533-585-18 [63533058518]

Han-I-Foam LIQUID
Marketing CategoryOTC monograph not final
Application Numberpart333
Product TypeHUMAN OTC DRUG
Marketing Start Date2009-09-01
Inactivation Date2020-01-31

NDC 63533-585-14 [63533058514]

Han-I-Foam LIQUID
Marketing CategoryOTC monograph not final
Application Numberpart333
Product TypeHUMAN OTC DRUG
Marketing Start Date2009-09-01
Inactivation Date2020-01-31

Drug Details

Active Ingredients

IngredientStrength
ALCOHOL.7 mL/mL

OpenFDA Data

SPL SET ID:6c1440b7-67fd-430d-9f6a-be0e0b098ac5
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 616805

    • NDC Crossover Matching brand name "Han-I-Foam" or generic name "Alcohol"

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    63533-855Han-I-FoamHan-I-Foam
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    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
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    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
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