NDC 63830-585

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 ID63830-585_b7297bc8-31de-44dd-978e-893af63a1b4a
NDC63830-585
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 Numberpart333
Labeler NamePro Chem, Incorporated
Substance NameALCOHOL
Active Ingredient Strength1 mL/mL
NDC Exclude FlagE
Listing Certified Through2018-12-31

Packaging

NDC 63830-585-11

1000 mL in 1 BOTTLE, PLASTIC (63830-585-11)
Marketing Start Date2009-09-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 63830-585-18 [63830058518]

Prevent LIQUID
Marketing CategoryOTC monograph not final
Application Numberpart333
Product TypeHUMAN OTC DRUG
Marketing Start Date2009-09-01
Inactivation Date2020-01-31

NDC 63830-585-03 [63830058503]

Prevent LIQUID
Marketing CategoryOTC monograph not final
Application Numberpart333
Product TypeHUMAN OTC DRUG
Marketing Start Date2009-09-01
Inactivation Date2020-01-31

NDC 63830-585-08 [63830058508]

Prevent LIQUID
Marketing CategoryOTC monograph not final
Application Numberpart333
Product TypeHUMAN OTC DRUG
Marketing Start Date2009-09-01
Inactivation Date2020-01-31

NDC 63830-585-07 [63830058507]

Prevent LIQUID
Marketing CategoryOTC monograph not final
Application Numberpart333
Product TypeHUMAN OTC DRUG
Marketing Start Date2009-09-01
Inactivation Date2020-01-31

NDC 63830-585-14 [63830058514]

Prevent LIQUID
Marketing CategoryOTC monograph not final
Application Numberpart333
Product TypeHUMAN OTC DRUG
Marketing Start Date2009-09-01
Inactivation Date2020-01-31

NDC 63830-585-12 [63830058512]

Prevent LIQUID
Marketing CategoryOTC monograph not final
Application Numberpart333
Product TypeHUMAN OTC DRUG
Marketing Start Date2009-09-01
Inactivation Date2020-01-31

NDC 63830-585-28 [63830058528]

Prevent LIQUID
Marketing CategoryOTC monograph not final
Application Numberpart333
Product TypeHUMAN OTC DRUG
Marketing Start Date2009-09-01
Inactivation Date2020-01-31

NDC 63830-585-01 [63830058501]

Prevent LIQUID
Marketing CategoryOTC monograph not final
Application Numberpart333
Product TypeHUMAN OTC DRUG
Marketing Start Date2009-09-01
Inactivation Date2020-01-31

NDC 63830-585-15 [63830058515]

Prevent LIQUID
Marketing CategoryOTC monograph not final
Application Numberpart333
Product TypeHUMAN OTC DRUG
Marketing Start Date2009-09-01
Inactivation Date2020-01-31

NDC 63830-585-16 [63830058516]

Prevent LIQUID
Marketing CategoryOTC monograph not final
Application Numberpart333
Product TypeHUMAN OTC DRUG
Marketing Start Date2009-09-01
Inactivation Date2020-01-31

NDC 63830-585-17 [63830058517]

Prevent LIQUID
Marketing CategoryOTC monograph not final
Application Numberpart333
Product TypeHUMAN OTC DRUG
Marketing Start Date2009-09-01
Inactivation Date2020-01-31

NDC 63830-585-06 [63830058506]

Prevent LIQUID
Marketing CategoryOTC monograph not final
Application Numberpart333
Product TypeHUMAN OTC DRUG
Marketing Start Date2009-09-01
Inactivation Date2020-01-31

NDC 63830-585-11 [63830058511]

Prevent LIQUID
Marketing CategoryOTC monograph not final
Application Numberpart333
Product TypeHUMAN OTC DRUG
Marketing Start Date2009-09-01
Inactivation Date2020-01-31

NDC 63830-585-05 [63830058505]

Prevent LIQUID
Marketing CategoryOTC monograph not final
Application Numberpart333
Product TypeHUMAN OTC DRUG
Marketing Start Date2009-09-01
Inactivation Date2020-01-31

NDC 63830-585-13 [63830058513]

Prevent LIQUID
Marketing CategoryOTC monograph not final
Application Numberpart333
Product TypeHUMAN OTC DRUG
Marketing Start Date2009-09-01
Inactivation Date2020-01-31

NDC 63830-585-10 [63830058510]

Prevent LIQUID
Marketing CategoryOTC monograph not final
Application Numberpart333
Product TypeHUMAN OTC DRUG
Marketing Start Date2009-09-01
Inactivation Date2020-01-31

NDC 63830-585-55 [63830058555]

Prevent LIQUID
Marketing CategoryOTC monograph not final
Application Numberpart333
Product TypeHUMAN OTC DRUG
Marketing Start Date2009-09-01
Inactivation Date2020-01-31

NDC 63830-585-09 [63830058509]

Prevent LIQUID
Marketing CategoryOTC monograph not final
Application Numberpart333
Product TypeHUMAN OTC DRUG
Marketing Start Date2009-09-01
Inactivation Date2020-01-31

NDC 63830-585-24 [63830058524]

Prevent LIQUID
Marketing CategoryOTC monograph not final
Application Numberpart333
Product TypeHUMAN OTC DRUG
Marketing Start Date2009-09-01
Inactivation Date2020-01-31

NDC 63830-585-27 [63830058527]

Prevent LIQUID
Marketing CategoryOTC monograph not final
Application Numberpart333
Product TypeHUMAN OTC DRUG
Marketing Start Date2009-09-01
Inactivation Date2020-01-31

Drug Details

Active Ingredients

IngredientStrength
ALCOHOL.7 mL/mL

OpenFDA Data

SPL SET ID:f48c62f9-04ad-48d5-bb69-d40ec83fdcf2
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 616805
  • 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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