MENTHOL

UNIISPL

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

Identification

ManufacturerSUNSET PAIN RELIEF

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
7293763203
90 mL in 1 BOTTLE, WITH APPLICATOR (72937-632-03)

Annotations

UNII (FDA Substance ID)

L7T10EIP3A

MENTHOL, UNSPECIFIED FORM

RxCUI 6750

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "L7T10EIP3A",
    "rxcui": "6750",
    "inchikey": null,
    "display_name": "MENTHOL, UNSPECIFIED FORM",
    "substance_type": "mixture",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "TOPICAL",
  "spl_meta": {
    "4a054949-0889-7182-e063-6394a90aff5e": {
      "match": "brand_token",
      "title": "MENTHOL PLUS CAMPHOR PAIN RELIEF (MENTHOL, CAMPHOR) SPRAY [VERIDIAN HEALTHCARE]",
      "spl_version": "2",
      "published_date": "2026-06-01"
    }
  },
  "productid": "72937-632_45c5ca7e-20df-92db-e063-6294a90ac402",
  "productndc": "72937-632",
  "dosage_form": "GEL",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "MENTHOL, UNSPECIFIED FORM",
  "proprietary_name": "MENTHOL",
  "active_ingred_unit": "g/100mL",
  "application_number": "M017",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "MENTHOL",
  "start_marketing_date": "20251220",
  "active_numerator_strength": "4"
}

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