Home NDC 72238-001 Vamousse Lice Treatment
Product NDC 72238-001
11-digit product format 722380001
Labeler code 72238
Product ID 72238-001_45371982-daac-f344-e063-6394a90a2f41
Type HUMAN OTC DRUG
Nonproprietary name Pediculicide
Dosage form AEROSOL, FOAM
Route TOPICAL
Labeler Alliance Pharma Inc.
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2018-10-01
Substance SODIUM CHLORIDE
Active strength 2 [hp_X]/mL
Pharmacologic classes Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Osmotic Activity [MoA], Osmotic Laxative [EPC]
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base Vamousse Lice Treatment
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength SODIUM CHLORIDE 2 [hp_X]/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 451W47IQ8X Internal UNII lookup
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 72238-001-01 Vamousse Lice Treatment 177 mL in 1 BOTTLE, WITH APPLICATOR AEROSOL, FOAM 177 10 72238-001-01 Vamousse Lice Treatment 1 in 1 BOX AEROSOL, FOAM 1 10
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 72238-001 VAMOUSSE LICE TREATMENT (PEDICULICIDE) AEROSOL, FOAM [ALLIANCE PHARMA INC.] 9 Current NDC, Legacy NDC, 2 package rows 20241013_75db3fab-5523-4880-e053-2a91aa0a925e.zip
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 1 of 1 · 1 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Marketing start Marketing end Sample Exclude flag Status 72238-001-01 72238000101 1 BOTTLE, WITH APPLICATOR in 1 BOX (72238-001-01) / 177 mL in 1 BOTTLE, WITH APPLICATOR 2018-10-01 0000-00-00 No No Current