Mouth Relief Liquid

SPL

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

Identification

ManufacturerShantou South Moon Biotechnology Co., Ltd.

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
8498303101
25 mg in 1 BOTTLE, PLASTIC (84983-031-01)

Annotations

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "route": "TOPICAL",
  "spl_meta": {
    "5264f81c-bffe-4f6d-e063-6394a90ae3bf": {
      "match": "brand_token",
      "title": "MOUTH ULCER (PANTHENOL) LIQUID [GUANGZHOU SHENGLI SHIDAI COSMETICS CO., LTD.]",
      "spl_version": "1",
      "published_date": "2026-05-26"
    }
  },
  "productid": "84983-031_508190ae-6314-b522-e063-6394a90a9c38",
  "productndc": "84983-031",
  "dosage_form": "LIQUID",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "MENTHA PIPERITA (PEPPERMINT) LEAF",
  "proprietary_name": "Mouth Relief Liquid",
  "active_ingred_unit": "mg/25mg",
  "application_number": "M016",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "GLYCERIN",
  "start_marketing_date": "20260428",
  "active_numerator_strength": ".075"
}

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