NDC 50519-738

Sani Spritz

Alcohol

Sani Spritz is a Topical Liquid in the Human Otc Drug category. It is labeled and distributed by American Industrial Supply, Inc.. The primary component is Alcohol.

Product ID50519-738_440f158e-0626-428e-9ad5-a49265926364
NDC50519-738
Product TypeHuman Otc Drug
Proprietary NameSani Spritz
Generic NameAlcohol
Dosage FormLiquid
Route of AdministrationTOPICAL
Marketing Start Date2009-12-31
Marketing CategoryOTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL
Application Numberpart333
Labeler NameAmerican Industrial Supply, Inc.
Substance NameALCOHOL
Active Ingredient Strength1 mL/mL
NDC Exclude FlagE
Listing Certified Through2017-12-31

Packaging

NDC 50519-738-14

3785 mL in 1 BOTTLE, PLASTIC (50519-738-14)
Marketing Start Date2009-12-31
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 50519-738-55 [50519073855]

Sani Spritz LIQUID
Marketing CategoryOTC monograph not final
Application Numberpart333
Product TypeHUMAN OTC DRUG
Marketing Start Date2009-12-31
Inactivation Date2019-10-21

NDC 50519-738-14 [50519073814]

Sani Spritz LIQUID
Marketing CategoryOTC monograph not final
Application Numberpart333
Product TypeHUMAN OTC DRUG
Marketing Start Date2009-12-31
Inactivation Date2019-10-21

NDC 50519-738-24 [50519073824]

Sani Spritz LIQUID
Marketing CategoryOTC monograph not final
Application Numberpart333
Product TypeHUMAN OTC DRUG
Marketing Start Date2009-12-31
Inactivation Date2019-10-21

NDC 50519-738-15 [50519073815]

Sani Spritz LIQUID
Marketing CategoryOTC monograph not final
Application Numberpart333
Product TypeHUMAN OTC DRUG
Marketing Start Date2009-12-31
Inactivation Date2019-10-21

NDC 50519-738-18 [50519073818]

Sani Spritz LIQUID
Marketing CategoryOTC monograph not final
Application Numberpart333
Product TypeHUMAN OTC DRUG
Marketing Start Date2009-12-31
Inactivation Date2019-10-21

NDC 50519-738-17 [50519073817]

Sani Spritz LIQUID
Marketing CategoryOTC monograph not final
Application Numberpart333
Product TypeHUMAN OTC DRUG
Marketing Start Date2009-12-31
Inactivation Date2019-10-21

NDC 50519-738-16 [50519073816]

Sani Spritz LIQUID
Marketing CategoryOTC monograph not final
Application Numberpart333
Product TypeHUMAN OTC DRUG
Marketing Start Date2009-12-31
Inactivation Date2019-10-21

Drug Details

Active Ingredients

IngredientStrength
ALCOHOL.7 mL/mL

OpenFDA Data

SPL SET ID:15089303-d145-4593-a459-13c661959124
Manufacturer
UNII

NDC Crossover Matching brand name "Sani Spritz" or generic name "Alcohol"

NDCBrand NameGeneric Name
50519-738Sani SpritzSani Spritz
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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