XIMONTH Quick Essence

UNIISPL

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

Identification

ManufacturerShantou Ximonth Biotechnology Co., Ltd.

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
8498901201
20 mg in 1 BOTTLE, GLASS (84989-012-01)

Annotations

UNII (FDA Substance ID)

V95R5KMY2B

PEPPERMINT

RxCUI 1010971

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "V95R5KMY2B",
    "rxcui": "1010971",
    "inchikey": null,
    "display_name": "PEPPERMINT",
    "substance_type": "structurallyDiverse",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "TOPICAL",
  "spl_meta": {
    "514a998d-aa2a-46b6-e063-6294a90a6c22": {
      "match": "brand_token",
      "title": "XIMONTH NAIL FUNGUS CARE LIQUID (GLYCERIN) LIQUID [SHANTOU XIMONTH BIOTECHNOLOGY CO., LTD.]",
      "spl_version": "1",
      "published_date": "2026-05-11"
    }
  },
  "productid": "84989-012_448b7147-f046-c50a-e063-6294a90a2f75",
  "productndc": "84989-012",
  "dosage_form": "LIQUID",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "PEPPERMINT; TEA TREE OIL; WITCH HAZEL",
  "proprietary_name": "XIMONTH Quick Essence",
  "active_ingred_unit": "mg/20mg; mg/20mg; mg/20mg",
  "application_number": "M028",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "Salicylic Acid",
  "start_marketing_date": "20251030",
  "active_numerator_strength": ".1; .04; .6"
}

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