Medicated Body

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 · 2

ndc11
5200003825
283 g in 1 BOTTLE (52000-038-25)
ndc11
5200003826
226 g in 1 BOTTLE (52000-038-26)

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": {
    "52d0b36c-b65e-00cf-e063-6294a90ad089": {
      "match": "brand_token",
      "title": "MEDICATED CALLUS REMOVERS (SALICYLIC ACID) PATCH [PREMIER BRANDS OF AMERICA INC]",
      "spl_version": "1",
      "published_date": "2026-05-28"
    }
  },
  "productid": "52000-038_6af56e16-5a14-4a8b-9491-6891be500637",
  "productndc": "52000-038",
  "dosage_form": "POWDER",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "MENTHOL, UNSPECIFIED FORM; ZINC OXIDE",
  "proprietary_name": "Medicated Body",
  "active_ingred_unit": "mg/g; mg/g",
  "application_number": "M016",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "Menthol and Zinc Oxide",
  "start_marketing_date": "20171204",
  "active_numerator_strength": "1.5; 10"
}

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