KENS PAIN AND ARTHRITIS FORMULA

UNIISPL

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

Identification

ManufacturerEezaway Relief Inc

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
6967814303
88 mL in 1 BOTTLE (69678-143-03)

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": {
    "35834473-3ad5-41ec-a110-e742aa7e2ee4": {
      "match": "brand_token",
      "title": "KENS PAIN AND ARTHRITIS FORMULA (MENTHOL) LIQUID [EEZAWAY RELIEF INC]",
      "spl_version": "2",
      "published_date": "2025-07-21"
    }
  },
  "productid": "69678-143_c01c4dab-9263-43d7-88dd-5df72403f96c",
  "productndc": "69678-143",
  "dosage_form": "LIQUID",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "MENTHOL, UNSPECIFIED FORM",
  "proprietary_name": "KENS PAIN AND ARTHRITIS FORMULA",
  "active_ingred_unit": "g/100mL",
  "application_number": "M017",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "MENTHOL",
  "start_marketing_date": "20240305",
  "active_numerator_strength": "2.75"
}

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