LCFateLC Nail Liquid

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
8498902401
30 mg in 1 BOTTLE, PLASTIC (84989-024-01)

Annotations

UNII (FDA Substance ID)

724GKU717M

JOJOBA OIL

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "724GKU717M",
    "rxcui": null,
    "inchikey": null,
    "display_name": "JOJOBA OIL",
    "substance_type": "structurallyDiverse",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "TOPICAL",
  "spl_meta": {
    "51ea23f4-0a23-4ae1-e063-6394a90aa051": {
      "match": "brand_token",
      "title": "LCFATELC NAIL LIQUID (GLYCERIN) LIQUID [SHANTOU XIMONTH BIOTECHNOLOGY CO., LTD.]",
      "spl_version": "1",
      "published_date": "2026-05-20"
    }
  },
  "productid": "84989-024_51ea23f4-0a24-4ae1-e063-6394a90aa051",
  "productndc": "84989-024",
  "dosage_form": "LIQUID",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "JOJOBA OIL; TEA TREE OIL",
  "proprietary_name": "LCFateLC Nail Liquid",
  "active_ingred_unit": "mg/30mg; mg/30mg",
  "application_number": "M016",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "GLYCERIN",
  "start_marketing_date": "20260516",
  "active_numerator_strength": ".003; .003"
}

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