Home NDC 72238-003-01 Vamousse Lice Treatment Complete Kit
Product NDC 72238-003
Requested package NDC 72238-003-01
11-digit product format 722380003
Labeler code 72238
Product ID 72238-003_45375277-eec9-34a3-e063-6394a90a581e
Type HUMAN OTC DRUG
Nonproprietary name sodium chloride and eucalyptus globulus leaf
Dosage form KIT
Route TOPICAL
Labeler Alliance Pharma Inc.
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2019-08-23
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes openFDA label cross-check# Cross-check layer: openFDA label JSON enriches search and identifies hydration gaps. The DailyMed Structured Product Label remains the canonical label presentation on FDA.report. Every label matching the complete exact-identifier union is deduplicated and paginated below.
Matched openFDA labels page 1 of 1 · 1 matching rows.
Additional Listing Data#
Finished product Yes
Brand name base Vamousse Lice Treatment Complete Kit
Listing expiration 2026-12-31 Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 72238-003-01 Vamousse Lice Treatment Complete Kit 1 in 1 BOX KIT 1 12
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 72238-003 VAMOUSSE LICE TREATMENT COMPLETE KIT (SODIUM CHLORIDE AND EUCALYPTUS GLOBULUS LEAF) KIT [ALLIANCE PHARMA INC.] 11 Current NDC, Legacy NDC, 1 package rows 20250224_90cffb2a-7be4-4f63-e053-2995a90a83f3.zip
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 72238-003-01 72238000301 1 KIT in 1 BOX (72238-003-01) * 1 mL in 1 BOTTLE, WITH APPLICATOR * 118 mL in 1 BOTTLE 1 kit 2019-08-23 0000-00-00 No No Current