NDC 63830-855

Prevent

Alcohol

Prevent is a Topical Liquid in the Human Otc Drug category. It is labeled and distributed by Pro Chem, Incorporated. The primary component is Alcohol.

Product ID63830-855_04592bcf-e266-4259-b798-ab97c0228414
NDC63830-855
Product TypeHuman Otc Drug
Proprietary NamePrevent
Generic NameAlcohol
Dosage FormLiquid
Route of AdministrationTOPICAL
Marketing Start Date2009-09-01
Marketing CategoryOTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL
Application Numberpart333E
Labeler NamePro Chem, Incorporated
Substance NameALCOHOL
Active Ingredient Strength1 mL/mL
NDC Exclude FlagN
Listing Certified Through2021-12-31

Packaging

NDC 63830-855-10

1000 mL in 1 CARTRIDGE (63830-855-10)
Marketing Start Date2019-07-08
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 63830-855-12 [63830085512]

Prevent LIQUID
Marketing CategoryOTC monograph not final
Application Numberpart333E
Product TypeHUMAN OTC DRUG
Marketing Start Date2009-09-01
Marketing End Date2018-12-04

NDC 63830-855-07 [63830085507]

Prevent LIQUID
Marketing CategoryOTC monograph not final
Application Numberpart333E
Product TypeHUMAN OTC DRUG
Marketing Start Date2009-09-01
Marketing End Date2018-12-04

NDC 63830-855-16 [63830085516]

Prevent LIQUID
Marketing CategoryOTC monograph not final
Application Numberpart333E
Product TypeHUMAN OTC DRUG
Marketing Start Date2009-09-01
Marketing End Date2018-12-04

NDC 63830-855-17 [63830085517]

Prevent LIQUID
Marketing CategoryOTC monograph not final
Application Numberpart333E
Product TypeHUMAN OTC DRUG
Marketing Start Date2019-07-08

NDC 63830-855-24 [63830085524]

Prevent LIQUID
Marketing CategoryOTC monograph not final
Application Numberpart333E
Product TypeHUMAN OTC DRUG
Marketing Start Date2019-07-08

NDC 63830-855-05 [63830085505]

Prevent LIQUID
Marketing CategoryOTC monograph not final
Application Numberpart333E
Product TypeHUMAN OTC DRUG
Marketing Start Date2009-09-01
Marketing End Date2018-12-04

NDC 63830-855-11 [63830085511]

Prevent LIQUID
Marketing CategoryOTC monograph not final
Application Numberpart333E
Product TypeHUMAN OTC DRUG
Marketing Start Date2009-09-01
Marketing End Date2018-12-04

NDC 63830-855-01 [63830085501]

Prevent LIQUID
Marketing CategoryOTC monograph not final
Application Numberpart333E
Product TypeHUMAN OTC DRUG
Marketing Start Date2009-09-01
Marketing End Date2018-12-04

NDC 63830-855-14 [63830085514]

Prevent LIQUID
Marketing CategoryOTC monograph not final
Application Numberpart333E
Product TypeHUMAN OTC DRUG
Marketing Start Date2019-07-08

NDC 63830-855-09 [63830085509]

Prevent LIQUID
Marketing CategoryOTC monograph not final
Application Numberpart333E
Product TypeHUMAN OTC DRUG
Marketing Start Date2009-09-01
Marketing End Date2018-12-04

NDC 63830-855-13 [63830085513]

Prevent LIQUID
Marketing CategoryOTC monograph not final
Application Numberpart333E
Product TypeHUMAN OTC DRUG
Marketing Start Date2009-09-01
Marketing End Date2018-12-04

NDC 63830-855-15 [63830085515]

Prevent LIQUID
Marketing CategoryOTC monograph not final
Application Numberpart333E
Product TypeHUMAN OTC DRUG
Marketing Start Date2009-09-01
Marketing End Date2018-12-04

NDC 63830-855-06 [63830085506]

Prevent LIQUID
Marketing CategoryOTC monograph not final
Application Numberpart333E
Product TypeHUMAN OTC DRUG
Marketing Start Date2009-09-01
Marketing End Date2018-12-04

NDC 63830-855-03 [63830085503]

Prevent LIQUID
Marketing CategoryOTC monograph not final
Application Numberpart333E
Product TypeHUMAN OTC DRUG
Marketing Start Date2009-09-01
Marketing End Date2018-12-04

NDC 63830-855-18 [63830085518]

Prevent LIQUID
Marketing CategoryOTC monograph not final
Application Numberpart333E
Product TypeHUMAN OTC DRUG
Marketing Start Date2019-07-08

NDC 63830-855-10 [63830085510]

Prevent LIQUID
Marketing CategoryOTC monograph not final
Application Numberpart333E
Product TypeHUMAN OTC DRUG
Marketing Start Date2019-07-08

NDC 63830-855-28 [63830085528]

Prevent LIQUID
Marketing CategoryOTC monograph not final
Application Numberpart333E
Product TypeHUMAN OTC DRUG
Marketing Start Date2019-07-08

NDC 63830-855-55 [63830085555]

Prevent LIQUID
Marketing CategoryOTC monograph not final
Application Numberpart333E
Product TypeHUMAN OTC DRUG
Marketing Start Date2009-09-01
Marketing End Date2018-12-04

NDC 63830-855-27 [63830085527]

Prevent LIQUID
Marketing CategoryOTC monograph not final
Application Numberpart333E
Product TypeHUMAN OTC DRUG
Marketing Start Date2009-09-01
Marketing End Date2018-12-04

NDC 63830-855-08 [63830085508]

Prevent LIQUID
Marketing CategoryOTC monograph not final
Application Numberpart333E
Product TypeHUMAN OTC DRUG
Marketing Start Date2009-09-01
Marketing End Date2018-12-04

Drug Details

Active Ingredients

IngredientStrength
ALCOHOL.62 mL/mL

OpenFDA Data

SPL SET ID:11b58699-8a04-43b7-8f69-3bf8b1d7addb
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 616763
  • NDC Crossover Matching brand name "Prevent" or generic name "Alcohol"

    NDCBrand NameGeneric Name
    63830-585PreventPrevent
    63830-855PreventPrevent
    66077-141PreventPrevent
    66077-708PreventPrevent
    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 [Prevent]

    Mark Image

    Registration | Serial
    Company
    Trademark
    Application Date
    PREVENT
    PREVENT
    98454598 not registered Live/Pending
    L'Oreal USA S/D, Inc.
    2024-03-18
    PREVENT
    PREVENT
    97788937 not registered Live/Pending
    Uhalley, David A
    2023-02-09
    PREVENT
    PREVENT
    97433705 not registered Live/Pending
    Clear Choice Therapeutics, Inc.
    2022-05-29
    PREVENT
    PREVENT
    90644844 not registered Live/Pending
    Chungyeon Sky Co., Ltd.
    2021-04-14
    PREVENT
    PREVENT
    90467411 not registered Live/Pending
    United States Salt, Inc.
    2021-01-14
    PREVENT
    PREVENT
    90369793 not registered Live/Pending
    Grass Pad, Inc.
    2020-12-09
    PREVENT
    PREVENT
    90369694 not registered Live/Pending
    Grass Pad, Inc.
    2020-12-09
    PREVENT
    PREVENT
    90041312 not registered Live/Pending
    Prevent LLC
    2020-07-08
    PREVENT
    PREVENT
    88630791 not registered Live/Pending
    Ortho8 Inc
    2019-09-25
    PREVENT
    PREVENT
    88366278 not registered Dead/Abandoned
    HPSRx Enterprises, Inc.
    2019-04-01
    PREVENT
    PREVENT
    88366260 not registered Dead/Abandoned
    HPSRx Enterprises, Inc.
    2019-04-01
    PREVENT
    PREVENT
    88103294 not registered Live/Pending
    Hubbell Incorporated
    2018-09-04

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