NDC 50519-221

Sani-Gel

Alcohol

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

Product ID50519-221_60c9f9c4-032c-45a3-85db-2239d362ccc5
NDC50519-221
Product TypeHuman Otc Drug
Proprietary NameSani-Gel
Generic NameAlcohol
Dosage FormGel
Route of AdministrationTOPICAL
Marketing Start Date2009-12-01
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 50519-221-11

1000 mL in 1 BOTTLE, PLASTIC (50519-221-11)
Marketing Start Date2009-12-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 50519-221-08 [50519022108]

Sani-Gel GEL
Marketing CategoryOTC monograph not final
Application Numberpart333
Product TypeHUMAN OTC DRUG
Marketing Start Date2009-12-01
Inactivation Date2019-10-21

NDC 50519-221-12 [50519022112]

Sani-Gel GEL
Marketing CategoryOTC monograph not final
Application Numberpart333
Product TypeHUMAN OTC DRUG
Marketing Start Date2009-12-01
Inactivation Date2019-10-21

NDC 50519-221-17 [50519022117]

Sani-Gel GEL
Marketing CategoryOTC monograph not final
Application Numberpart333
Product TypeHUMAN OTC DRUG
Marketing Start Date2009-12-01
Inactivation Date2019-10-21

NDC 50519-221-09 [50519022109]

Sani-Gel GEL
Marketing CategoryOTC monograph not final
Application Numberpart333
Product TypeHUMAN OTC DRUG
Marketing Start Date2009-12-01
Inactivation Date2019-10-21

NDC 50519-221-27 [50519022127]

Sani-Gel GEL
Marketing CategoryOTC monograph not final
Application Numberpart333
Product TypeHUMAN OTC DRUG
Marketing Start Date2009-12-01
Inactivation Date2019-10-21

NDC 50519-221-01 [50519022101]

Sani-Gel GEL
Marketing CategoryOTC monograph not final
Application Numberpart333
Product TypeHUMAN OTC DRUG
Marketing Start Date2009-12-01
Inactivation Date2019-10-21

NDC 50519-221-06 [50519022106]

Sani-Gel GEL
Marketing CategoryOTC monograph not final
Application Numberpart333
Product TypeHUMAN OTC DRUG
Marketing Start Date2009-12-01
Inactivation Date2019-10-21

NDC 50519-221-05 [50519022105]

Sani-Gel GEL
Marketing CategoryOTC monograph not final
Application Numberpart333
Product TypeHUMAN OTC DRUG
Marketing Start Date2009-12-01
Inactivation Date2019-10-21

NDC 50519-221-11 [50519022111]

Sani-Gel GEL
Marketing CategoryOTC monograph not final
Application Numberpart333
Product TypeHUMAN OTC DRUG
Marketing Start Date2009-12-01
Inactivation Date2019-10-21

NDC 50519-221-07 [50519022107]

Sani-Gel GEL
Marketing CategoryOTC monograph not final
Application Numberpart333
Product TypeHUMAN OTC DRUG
Marketing Start Date2009-12-01
Inactivation Date2019-10-21

NDC 50519-221-28 [50519022128]

Sani-Gel GEL
Marketing CategoryOTC monograph not final
Application Numberpart333
Product TypeHUMAN OTC DRUG
Marketing Start Date2009-12-01
Inactivation Date2019-10-21

NDC 50519-221-13 [50519022113]

Sani-Gel GEL
Marketing CategoryOTC monograph not final
Application Numberpart333
Product TypeHUMAN OTC DRUG
Marketing Start Date2009-12-01
Inactivation Date2019-10-21

NDC 50519-221-10 [50519022110]

Sani-Gel GEL
Marketing CategoryOTC monograph not final
Application Numberpart333
Product TypeHUMAN OTC DRUG
Marketing Start Date2009-12-01
Inactivation Date2019-10-21

NDC 50519-221-03 [50519022103]

Sani-Gel GEL
Marketing CategoryOTC monograph not final
Application Numberpart333
Product TypeHUMAN OTC DRUG
Marketing Start Date2009-12-01
Inactivation Date2019-10-21

NDC 50519-221-55 [50519022155]

Sani-Gel GEL
Marketing CategoryOTC monograph not final
Application Numberpart333
Product TypeHUMAN OTC DRUG
Marketing Start Date2009-12-01
Inactivation Date2019-10-21

NDC 50519-221-14 [50519022114]

Sani-Gel GEL
Marketing CategoryOTC monograph not final
Application Numberpart333
Product TypeHUMAN OTC DRUG
Marketing Start Date2009-12-01
Inactivation Date2019-10-21

NDC 50519-221-15 [50519022115]

Sani-Gel GEL
Marketing CategoryOTC monograph not final
Application Numberpart333
Product TypeHUMAN OTC DRUG
Marketing Start Date2009-12-01
Inactivation Date2019-10-21

NDC 50519-221-24 [50519022124]

Sani-Gel GEL
Marketing CategoryOTC monograph not final
Application Numberpart333
Product TypeHUMAN OTC DRUG
Marketing Start Date2009-12-01
Inactivation Date2019-10-21

Drug Details

Active Ingredients

IngredientStrength
ALCOHOL.7 mL/mL

OpenFDA Data

SPL SET ID:b9d34ee8-896c-464d-b4fc-a1d844bf4b3f
Manufacturer
UNII

NDC Crossover Matching brand name "Sani-Gel" or generic name "Alcohol"

NDCBrand NameGeneric Name
50519-221Sani-GelSani-Gel
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

Trademark Results [Sani-Gel]

Mark Image

Registration | Serial
Company
Trademark
Application Date
SANI-GEL
SANI-GEL
75240816 2231386 Live/Registered
ENERGIZER BRANDS II LLC
1997-01-21
SANI-GEL
SANI-GEL
74302763 not registered Dead/Abandoned
Tec Laboratories, Inc.
1992-08-10

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