NDC 61924-093

KLEENFOAM

Otc Antimicrobial Drug Product

KLEENFOAM is a Topical Aerosol, Foam in the Human Otc Drug category. It is labeled and distributed by Dermarite Industries Llc. The primary component is Chloroxylenol.

Product ID61924-093_75d5611a-f9d4-1841-e053-2991aa0af415
NDC61924-093
Product TypeHuman Otc Drug
Proprietary NameKLEENFOAM
Generic NameOtc Antimicrobial Drug Product
Dosage FormAerosol, Foam
Route of AdministrationTOPICAL
Marketing Start Date2011-12-12
Marketing CategoryOTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL
Application Numberpart333A
Labeler NameDermarite Industries LLC
Substance NameCHLOROXYLENOL
Active Ingredient Strength0 g/mL
NDC Exclude FlagN
Listing Certified Through2019-12-31

Packaging

NDC 61924-093-34

1000 mL in 1 CARTRIDGE (61924-093-34)
Marketing Start Date2011-12-12
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 61924-093-34 [61924009334]

KLEENFOAM AEROSOL, FOAM
Marketing CategoryOTC monograph not final
Application Numberpart333A
Product TypeHUMAN OTC DRUG
Marketing Start Date2011-12-12

Drug Details

Active Ingredients

IngredientStrength
CHLOROXYLENOL.005 g/mL

OpenFDA Data

SPL SET ID:f4ea9ae8-c783-48b4-af31-a26ecaa34992
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 1550947
    • UPC Code
  • 0714196093349

    • Trademark Results [KLEENFOAM]

    Mark Image

    Registration | Serial
    Company
    Trademark
    Application Date
    KLEENFOAM
    KLEENFOAM
    87129012 5170260 Live/Registered
    National Refrigeration & Air Conditioning Products, Inc.
    2016-08-05
    KLEENFOAM
    KLEENFOAM
    77372922 3592611 Dead/Cancelled
    DermaRite Industries, LLC
    2008-01-16
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