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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
- ndc117223800402118 mL in 1 BOTTLE (72238-004-02)
- ndc117223800403400 mL in 1 BOTTLE (72238-004-03)
- ndc117223800405250 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"
}Access this data programmatically
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