Muscle Rub Pain Reliever Gel

UNIISPL

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

Identification

ManufacturerUniversal Distribution Centre LLC

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
5200007204
1 TUBE in 1 CARTON (52000-072-04) / 35.4 g in 1 TUBE (52000-072-03)

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": {
    "163ba925-b26a-4737-8c05-68875435452b": {
      "match": "brand_token",
      "title": "MUSCLE RUB (MENTHOL, METHYL SALICYLATE) CREAM [ALDERMED INC.]",
      "spl_version": "5",
      "published_date": "2026-05-11"
    }
  },
  "productid": "52000-072_db1541b7-b2be-4751-a391-f0966f834ca3",
  "productndc": "52000-072",
  "dosage_form": "GEL",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "MENTHOL, UNSPECIFIED FORM",
  "proprietary_name": "Muscle Rub Pain Reliever Gel",
  "active_ingred_unit": "mg/g",
  "application_number": "M017",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "MENTHOL, UNSPECIFIED FORM",
  "start_marketing_date": "20210124",
  "active_numerator_strength": "25"
}

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