PAIN-X

UNIISPL

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

Identification

ManufacturerOL PHARMA TECH,LLC

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 2

ndc11
8048900301
1 TUBE in 1 CARTON (80489-003-01) / 28.3 g in 1 TUBE
ndc11
8048900302
1 TUBE in 1 CARTON (80489-003-02) / 49.6 g in 1 TUBE

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": {
    "b22bb19a-14e5-3d32-e053-2a95a90ae520": {
      "match": "brand_token",
      "title": "PAIN-X (MENTHOL) GEL [OL PHARMA TECH,LLC]",
      "spl_version": "4",
      "published_date": "2025-01-13"
    }
  },
  "productid": "80489-003_2b51e8c1-1805-573d-e063-6294a90a2f58",
  "productndc": "80489-003",
  "dosage_form": "GEL",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "MENTHOL, UNSPECIFIED FORM",
  "proprietary_name": "PAIN-X",
  "active_ingred_unit": "mg/g",
  "application_number": "M017",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "MENTHOL",
  "start_marketing_date": "20210101",
  "active_numerator_strength": "25"
}

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