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United States · US · US:72238-004_23fcd746-aca1-d666-e063-6394a90a62a5

Vamousse Lice Defense

UNIISPL

Last synced from FDA National Drug Code directory (United States) on

Identification

ManufacturerAlliance Pharma Inc.
CountryUS (United States)
ATC code
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 3

  • ndc11
    7223800402
    118 mL in 1 BOTTLE (72238-004-02)
  • ndc11
    7223800403
    400 mL in 1 BOTTLE (72238-004-03)
  • ndc11
    7223800405
    250 mL in 1 BOTTLE (72238-004-05)

Annotations

UNII (FDA Substance ID)
S546YLW6E6
EUCALYPTUS GLOBULUS LEAF
RxCUI 1305545
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
  "unii": {
    "unii": "S546YLW6E6",
    "rxcui": "1305545",
    "inchikey": null,
    "display_name": "EUCALYPTUS GLOBULUS LEAF",
    "substance_type": "structurallyDiverse",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "TOPICAL",
  "spl_meta": {
    "90cffb2a-7be4-4f63-e053-2995a90a83f3": {
      "match": "brand_token",
      "title": "VAMOUSSE LICE TREATMENT COMPLETE KIT (SODIUM CHLORIDE AND EUCALYPTUS GLOBULUS LEAF) KIT [ALLIANCE PHARMA INC.]",
      "spl_version": "12",
      "published_date": "2025-12-08"
    }
  },
  "productid": "72238-004_23fcd746-aca1-d666-e063-6394a90a62a5",
  "productndc": "72238-004",
  "dosage_form": "SHAMPOO",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "EUCALYPTUS GLOBULUS LEAF; SODIUM CHLORIDE",
  "proprietary_name": "Vamousse Lice Defense",
  "active_ingred_unit": "[hp_X]/mL; [hp_X]/mL",
  "application_number": null,
  "marketing_category": "UNAPPROVED HOMEOPATHIC",
  "nonproprietary_name": "Eucalyptus globulus, Natrum muriaticum",
  "start_marketing_date": "20210501",
  "active_numerator_strength": "2; 2"
}

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