NDC 72238-001

Vamousse Lice Treatment

Pediculicide

Vamousse Lice Treatment is a Topical Aerosol, Foam in the Human Otc Drug category. It is labeled and distributed by Alliance Pharma Inc.. The primary component is Sodium Chloride.

• Product ID: 72238-001_75db3fab-5524-4880-e053-2a91aa0a925e
• NDC: 72238-001
• Product Type: Human Otc Drug
• Proprietary Name: Vamousse Lice Treatment
• Generic Name: Pediculicide
• Dosage Form: Aerosol, Foam
• Route of Administration: TOPICAL
• Marketing Start Date: 2018-10-01
• Marketing Category: UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
• Labeler Name: Alliance Pharma Inc.
• Substance Name: SODIUM CHLORIDE
• Active Ingredient Strength: 2 [hp_X]/mL
• NDC Exclude Flag: N
• Listing Certified Through: 2019-12-31

Packaging

NDC 72238-001-01

1 BOTTLE, WITH APPLICATOR in 1 BOX (72238-001-01) > 177 mL in 1 BOTTLE, WITH APPLICATOR

• Marketing Start Date: 2018-10-01
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 72238-001-01 [72238000101]

Vamousse Lice Treatment AEROSOL, FOAM

• Marketing Category: unapproved homeopathic
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2018-10-01

Drug Details

Active Ingredients

Ingredient	Strength
SODIUM CHLORIDE	2 [hp_X]/mL

OpenFDA Data

• SPL SET ID: 75db3fab-5523-4880-e053-2a91aa0a925e
• Manufacturer:
  • Alliance Pharma Inc.
• UNII:
  • 451W47IQ8X

NDC Crossover Matching brand name "Vamousse Lice Treatment" or generic name "Pediculicide"

NDC	Brand Name	Generic Name
58962-002	Vamousse Lice Treatment	Sodium Chloride
72238-001	Vamousse Lice Treatment	Pediculicide
72238-002	Vamousse Lice Defense	Pediculicide