2.5% Menthol PAIN RELIEF

UNIISPL

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

Identification

ManufacturerUniversal Distribution Center LLC

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
5200044002
1 TUBE in 1 BOX (52000-440-02) / 57 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": {
    "8075ba60-772c-4d1a-8584-722bb3e539be": {
      "match": "brand_token",
      "title": "2.5% MENTHOL PAIN RELIEF (MENTHOL) GEL [NANTONG HEALTH & BEYOND HYGIENIC PRODUCTS INC.]",
      "spl_version": "1",
      "published_date": "2026-02-09"
    }
  },
  "productid": "52000-440_8b302a49-b577-429b-b508-b386e56c2af3",
  "productndc": "52000-440",
  "dosage_form": "GEL",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "MENTHOL, UNSPECIFIED FORM",
  "proprietary_name": "2.5% Menthol PAIN RELIEF",
  "active_ingred_unit": "mg/g",
  "application_number": "M017",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "Menthol",
  "start_marketing_date": "20260119",
  "active_numerator_strength": "25"
}

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