foamgle foam mouthwash super mint

Generic: allantoin

Labeler: kmpharmaceutical co.,ltd
NDC Directory HUMAN OTC DRUG UNAPPROVED DRUG OTHER Inactive Finished

Drug Facts

Product Profile

Brand Name foamgle foam mouthwash super mint
Generic Name allantoin
Labeler kmpharmaceutical co.,ltd
Dosage Form LIQUID
Routes
ORAL
Active Ingredients

allantoin .05 g/100mL

Manufacturer
KMPHARMACEUTICAL CO.,LTD

Identifiers & Regulatory

Product NDC 50555-210
Product ID 50555-210_352342bf-e2de-3a2c-e063-6294a90a200e
Product Type HUMAN OTC DRUG
Marketing Category UNAPPROVED DRUG OTHER
Listing Expiration 2026-12-31
Marketing Start 2025-05-01

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 50555210
Hyphenated Format 50555-210

Supplemental Identifiers

UNII
344S277G0Z

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name foamgle foam mouthwash super mint (source: ndc)
Generic Name allantoin (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • .05 g/100mL
source: ndc
Packaging
  • 1 BOTTLE in 1 CARTON (50555-210-02) / 50 mL in 1 BOTTLE (50555-210-01)
source: ndc

Packages (1)

Ingredients (1)

allantoin (.05 g/100mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "352342bf-e2de-3a2c-e063-6294a90a200e", "openfda": {"unii": ["344S277G0Z"], "spl_set_id": ["352342bf-e2dd-3a2c-e063-6294a90a200e"], "manufacturer_name": ["KMPHARMACEUTICAL CO.,LTD"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (50555-210-02)  / 50 mL in 1 BOTTLE (50555-210-01)", "package_ndc": "50555-210-02", "marketing_start_date": "20250501"}], "brand_name": "Foamgle Foam Mouthwash Super Mint", "product_id": "50555-210_352342bf-e2de-3a2c-e063-6294a90a200e", "dosage_form": "LIQUID", "product_ndc": "50555-210", "generic_name": "Allantoin", "labeler_name": "KMPHARMACEUTICAL CO.,LTD", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Foamgle Foam Mouthwash Super Mint", "active_ingredients": [{"name": "ALLANTOIN", "strength": ".05 g/100mL"}], "marketing_category": "UNAPPROVED DRUG OTHER", "marketing_start_date": "20250501", "listing_expiration_date": "20261231"}