Foamgle Foam Mouthwash Super Mint

UNIISPL

Last synced from FDA National Drug Code directory (United States) on June 3, 2026

Identification

ManufacturerKMPHARMACEUTICAL CO.,LTD

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
5055521002
1 BOTTLE in 1 CARTON (50555-210-02) / 50 mL in 1 BOTTLE (50555-210-01)

Annotations

UNII (FDA Substance ID)

344S277G0Z

ALLANTOIN

RxCUI 508

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "344S277G0Z",
    "rxcui": "508",
    "inchikey": "POJWUDADGALRAB-UHFFFAOYSA-N",
    "display_name": "ALLANTOIN",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "4c006ee3-bf69-e65c-e063-6294a90a4b96": {
      "match": "brand_token",
      "title": "FOAMGLE FOAM SUPER MINT (ALLANTOIN) MOUTHWASH [KMPHARMACEUTICAL CO.,LTD]",
      "spl_version": "1",
      "published_date": "2026-03-02"
    }
  },
  "productid": "50555-210_352342bf-e2de-3a2c-e063-6294a90a200e",
  "productndc": "50555-210",
  "dosage_form": "LIQUID",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "ALLANTOIN",
  "proprietary_name": "Foamgle Foam Mouthwash Super Mint",
  "active_ingred_unit": "g/100mL",
  "application_number": null,
  "marketing_category": "UNAPPROVED DRUG OTHER",
  "nonproprietary_name": "Allantoin",
  "start_marketing_date": "20250501",
  "active_numerator_strength": ".05"
}

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