NDC11 72238000301

This exact 11-digit normalized identifier can correspond to more than one FDA hyphenation. FDA.report preserves the exact identifier and exposes every structurally valid candidate without guessing.

Possible FDA NDC forms#

Package NDC, Product root table
Package NDC	Product root
72238-0003-01	72238-0003
72238-0003-1	72238-0003
72238-003-01	72238-003

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.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Vamousse Lice Treatment Complete Kit	SODIUM CHLORIDE AND EUCALYPTUS GLOBULUS LEAF	Alliance Pharma Inc.	90cffb2a-7be4-4f63-e053-2995a90a83f3	2025-12-05	Warnings	Exact identifier ndc (package): 72238-003-01 ndc (product): 72238-003 ndc11 (package): 72238000301

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.