NDC 50452-221

Pure Gel

Alcohol

Pure Gel is a Topical Gel in the Human Otc Drug category. It is labeled and distributed by Phoenix Research Industries, Inc.. The primary component is Alcohol.

Product ID50452-221_6587cd4a-676b-4a03-b5ad-14006c19a37c
NDC50452-221
Product TypeHuman Otc Drug
Proprietary NamePure Gel
Generic NameAlcohol
Dosage FormGel
Route of AdministrationTOPICAL
Marketing Start Date2010-02-01
Marketing CategoryOTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL
Application Numberpart333
Labeler NamePhoenix Research Industries, Inc.
Substance NameALCOHOL
Active Ingredient Strength1 mL/mL
NDC Exclude FlagE
Listing Certified Through2017-12-31

Packaging

NDC 50452-221-28

149 mL in 1 BOTTLE, PLASTIC (50452-221-28)
Marketing Start Date2010-02-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 50452-221-28 [50452022128]

Pure Gel GEL
Marketing CategoryOTC monograph not final
Application Numberpart333
Product TypeHUMAN OTC DRUG
Marketing Start Date2010-02-01
Inactivation Date2019-10-21

NDC 50452-221-03 [50452022103]

Pure Gel GEL
Marketing CategoryOTC monograph not final
Application Numberpart333
Product TypeHUMAN OTC DRUG
Marketing Start Date2010-02-01
Inactivation Date2019-10-21

NDC 50452-221-27 [50452022127]

Pure Gel GEL
Marketing CategoryOTC monograph not final
Application Numberpart333
Product TypeHUMAN OTC DRUG
Marketing Start Date2010-02-01
Inactivation Date2019-10-21

NDC 50452-221-12 [50452022112]

Pure Gel GEL
Marketing CategoryOTC monograph not final
Application Numberpart333
Product TypeHUMAN OTC DRUG
Marketing Start Date2010-02-01
Inactivation Date2019-10-21

NDC 50452-221-09 [50452022109]

Pure Gel GEL
Marketing CategoryOTC monograph not final
Application Numberpart333
Product TypeHUMAN OTC DRUG
Marketing Start Date2010-02-01
Inactivation Date2019-10-21

NDC 50452-221-14 [50452022114]

Pure Gel GEL
Marketing CategoryOTC monograph not final
Application Numberpart333
Product TypeHUMAN OTC DRUG
Marketing Start Date2010-02-01
Inactivation Date2019-10-21

NDC 50452-221-06 [50452022106]

Pure Gel GEL
Marketing CategoryOTC monograph not final
Application Numberpart333
Product TypeHUMAN OTC DRUG
Marketing Start Date2010-02-01
Inactivation Date2019-10-21

NDC 50452-221-15 [50452022115]

Pure Gel GEL
Marketing CategoryOTC monograph not final
Application Numberpart333
Product TypeHUMAN OTC DRUG
Marketing Start Date2010-02-01
Inactivation Date2019-10-21

NDC 50452-221-17 [50452022117]

Pure Gel GEL
Marketing CategoryOTC monograph not final
Application Numberpart333
Product TypeHUMAN OTC DRUG
Marketing Start Date2010-02-01
Inactivation Date2019-10-21

NDC 50452-221-01 [50452022101]

Pure Gel GEL
Marketing CategoryOTC monograph not final
Application Numberpart333
Product TypeHUMAN OTC DRUG
Marketing Start Date2010-02-01
Inactivation Date2019-10-21

NDC 50452-221-24 [50452022124]

Pure Gel GEL
Marketing CategoryOTC monograph not final
Application Numberpart333
Product TypeHUMAN OTC DRUG
Marketing Start Date2010-02-01
Inactivation Date2019-10-21

NDC 50452-221-13 [50452022113]

Pure Gel GEL
Marketing CategoryOTC monograph not final
Application Numberpart333
Product TypeHUMAN OTC DRUG
Marketing Start Date2010-02-01
Inactivation Date2019-10-21

NDC 50452-221-55 [50452022155]

Pure Gel GEL
Marketing CategoryOTC monograph not final
Application Numberpart333
Product TypeHUMAN OTC DRUG
Marketing Start Date2010-02-01
Inactivation Date2019-10-21

NDC 50452-221-10 [50452022110]

Pure Gel GEL
Marketing CategoryOTC monograph not final
Application Numberpart333
Product TypeHUMAN OTC DRUG
Marketing Start Date2010-02-01
Inactivation Date2019-10-21

NDC 50452-221-05 [50452022105]

Pure Gel GEL
Marketing CategoryOTC monograph not final
Application Numberpart333
Product TypeHUMAN OTC DRUG
Marketing Start Date2010-02-01
Inactivation Date2019-10-21

NDC 50452-221-08 [50452022108]

Pure Gel GEL
Marketing CategoryOTC monograph not final
Application Numberpart333
Product TypeHUMAN OTC DRUG
Marketing Start Date2010-02-01
Inactivation Date2019-10-21

NDC 50452-221-07 [50452022107]

Pure Gel GEL
Marketing CategoryOTC monograph not final
Application Numberpart333
Product TypeHUMAN OTC DRUG
Marketing Start Date2010-02-01
Inactivation Date2019-10-21

NDC 50452-221-11 [50452022111]

Pure Gel GEL
Marketing CategoryOTC monograph not final
Application Numberpart333
Product TypeHUMAN OTC DRUG
Marketing Start Date2010-02-01
Inactivation Date2019-10-21

Drug Details

Active Ingredients

IngredientStrength
ALCOHOL.7 mL/mL

OpenFDA Data

SPL SET ID:db41db60-23e2-4a3b-a151-d6306ddfb924
Manufacturer
UNII

NDC Crossover Matching brand name "Pure Gel" or generic name "Alcohol"

NDCBrand NameGeneric Name
50452-221Pure GelPure 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
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