United States · FDA National Drug Code directory
Foamgle Foam Super Mint
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 50555-220_4c006ee3-bf6a-e65c-e063-6294a90a4b96
- Product NDC
- 50555-220
- Form
- MOUTHWASH
- Composition / generic term
- Allantoin
- Labeler
- KMPHARMACEUTICAL CO.,LTD
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start / end (source format)
- 20260201
- Source listing expiry
- 20271231
Source-listed ingredients
- ALLANTOIN — .05 g/100mL
These values do not establish equivalence or a dose recommendation.
Packages
- 1 BOTTLE in 1 CARTON (50555-220-02) / 150 mL in 1 BOTTLE (50555-220-01) · 50555-220-02
Source and coverage
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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
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