NDC 76063-738

Handi-Sani

Alcohol

Handi-Sani is a Topical Liquid in the Human Otc Drug category. It is labeled and distributed by Chromate Industrial Corporation. The primary component is Alcohol.

Product ID76063-738_fb0a4a4e-74e6-4d6d-ac52-ff2ea95e061b
NDC76063-738
Product TypeHuman Otc Drug
Proprietary NameHandi-Sani
Generic NameAlcohol
Dosage FormLiquid
Route of AdministrationTOPICAL
Marketing Start Date2011-02-01
Marketing CategoryOTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL
Application Numberpart333E
Labeler NameChromate Industrial Corporation
Substance NameALCOHOL
Active Ingredient Strength1 mL/mL
NDC Exclude FlagE
Listing Certified Through2017-12-31

Packaging

NDC 76063-738-55

208200 mL in 1 DRUM (76063-738-55)
Marketing Start Date2011-02-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 76063-738-16 [76063073816]

Handi-Sani LIQUID
Marketing CategoryOTC monograph not final
Application Numberpart333E
Product TypeHUMAN OTC DRUG
Marketing Start Date2011-02-01
Inactivation Date2019-10-29

NDC 76063-738-15 [76063073815]

Handi-Sani LIQUID
Marketing CategoryOTC monograph not final
Application Numberpart333E
Product TypeHUMAN OTC DRUG
Marketing Start Date2011-02-01
Inactivation Date2019-10-29

NDC 76063-738-55 [76063073855]

Handi-Sani LIQUID
Marketing CategoryOTC monograph not final
Application Numberpart333E
Product TypeHUMAN OTC DRUG
Marketing Start Date2011-02-01
Inactivation Date2019-10-29

NDC 76063-738-17 [76063073817]

Handi-Sani LIQUID
Marketing CategoryOTC monograph not final
Application Numberpart333E
Product TypeHUMAN OTC DRUG
Marketing Start Date2011-02-01
Inactivation Date2019-10-29

NDC 76063-738-14 [76063073814]

Handi-Sani LIQUID
Marketing CategoryOTC monograph not final
Application Numberpart333E
Product TypeHUMAN OTC DRUG
Marketing Start Date2011-02-01
Inactivation Date2019-10-29

NDC 76063-738-18 [76063073818]

Handi-Sani LIQUID
Marketing CategoryOTC monograph not final
Application Numberpart333E
Product TypeHUMAN OTC DRUG
Marketing Start Date2011-02-01
Inactivation Date2019-10-29

NDC 76063-738-24 [76063073824]

Handi-Sani LIQUID
Marketing CategoryOTC monograph not final
Application Numberpart333E
Product TypeHUMAN OTC DRUG
Marketing Start Date2011-02-01
Inactivation Date2019-10-29

Drug Details

Active Ingredients

IngredientStrength
ALCOHOL.7 mL/mL

OpenFDA Data

SPL SET ID:a34f6387-305a-4d51-924f-8b7d11231ca3
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 247835

    • NDC Crossover Matching brand name "Handi-Sani" or generic name "Alcohol"

    NDCBrand NameGeneric Name
    76063-738Handi-SaniHandi-Sani
    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
    © 2024 FDA.report
    This site is not affiliated with or endorsed by the FDA.