Home NDC 50555-220 Foamgle Foam Super Mint
Product NDC 50555-220
11-digit product format 505550220
Labeler code 50555
Product ID 50555-220_4c006ee3-bf6a-e65c-e063-6294a90a4b96
Type HUMAN OTC DRUG
Nonproprietary name Allantoin
Dosage form MOUTHWASH
Route ORAL
Labeler KMPHARMACEUTICAL CO.,LTD
Marketing category UNAPPROVED DRUG OTHER
Marketing start 2026-02-01
Substance ALLANTOIN
Active strength .05 g/100mL
NDC exclude flag No
Listing certified through 2027-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base Foamgle Foam Super Mint
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ALLANTOIN .05 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 Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 50555-220-01 Foamgle Foam Super Mint 150 mL in 1 BOTTLE MOUTHWASH 150 1 50555-220-02 Foamgle Foam Super Mint 1 in 1 CARTON MOUTHWASH 1 1
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 50555-220-01 50555022001 150 mL in 1 BOTTLE 150 ml Historical 50555-220-02 50555022002 1 BOTTLE in 1 CARTON (50555-220-02) / 150 mL in 1 BOTTLE (50555-220-01) 1 bottle 2026-02-01 No No Current