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 ID: 61924-093_75d5611a-f9d4-1841-e053-2991aa0af415
• NDC: 61924-093
• Product Type: Human Otc Drug
• Proprietary Name: KLEENFOAM
• Generic Name: Otc Antimicrobial Drug Product
• Dosage Form: Aerosol, Foam
• Route of Administration: TOPICAL
• Marketing Start Date: 2011-12-12
• Marketing Category: OTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL
• Application Number: part333A
• Labeler Name: Dermarite Industries LLC
• Substance Name: CHLOROXYLENOL
• Active Ingredient Strength: 0 g/mL
• NDC Exclude Flag: N
• Listing Certified Through: 2019-12-31

Packaging

NDC 61924-093-34

1000 mL in 1 CARTRIDGE (61924-093-34)

• Marketing Start Date: 2011-12-12
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 61924-093-34 [61924009334]

KLEENFOAM AEROSOL, FOAM

• Marketing Category: OTC monograph not final
• Application Number: part333A
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2011-12-12

Drug Details

Active Ingredients

Ingredient	Strength
CHLOROXYLENOL	.005 g/mL

OpenFDA Data

• SPL SET ID: f4ea9ae8-c783-48b4-af31-a26ecaa34992
• Manufacturer:
  • Dermarite Industries LLC
• UNII:
  • 0F32U78V2Q
• RxNorm Concept Unique ID - RxCUI:
  • 1550947
• UPC Code:
  • 0714196093349