Home NDC 74196-0011 LESONEL FEMININE FOAMING WASH
Product NDC 74196-0011
11-digit product format 741960011
Labeler code 74196
Product ID 74196-0011_3033bf9e-0e48-de43-e063-6394a90ab14d
Type HUMAN OTC DRUG
Nonproprietary name ALLANTOIN
Dosage form LIQUID
Route VAGINAL
Labeler ACE PHARMACEUTICAL CO.,LTD.
Marketing category UNAPPROVED DRUG OTHER
Marketing start 2025-01-01
Substance ALLANTOIN
Active strength .1 g/100mL
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base LESONEL FEMININE FOAMING WASH
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ALLANTOIN .1 g/100mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 344S277G0Z Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 74196-0011-1 LESONEL FEMININE FOAMING WASH 300 mL in 1 BOTTLE, PUMP LIQUID 300 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 74196-0011 LESONEL FEMININE FOAMING WASH (ALLANTOIN) LIQUID [ACE PHARMACEUTICAL CO.,LTD.] 1 Current NDC, 1 package rows 20250315_3033b1b3-21b7-9b5b-e063-6294a90a54c5.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 Units Marketing start Sample Exclude flag Status 74196-0011-1 74196001101 300 mL in 1 BOTTLE, PUMP (74196-0011-1) 300 ml 2025-01-01 No No Current