MENTHOL

UNIISPL

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

Identification

ManufacturerSUNSET PAIN RELIEF ROLL-ON 3OZ

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
7293700403
90 mL in 1 BOTTLE, WITH APPLICATOR (72937-004-03)

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": "72937-004_44141d2a-1d91-b970-e063-6294a90a53f4",
  "productndc": "72937-004",
  "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": "20190924",
  "active_numerator_strength": "4"
}

Access this data programmatically

Query MENTHOL and 610,000+ other drug records through a single REST API — with a last_synced_at provenance stamp on every response. Free tier includes 100 requests/day.

Get a free API key Read the API docs