Ultra Strength Topical Pain Relief Cream

UNIISPL

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

Identification

ManufacturerJ C UDEOZOR & SONS GLOBAL INDUSTRIES LTD

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
8272900601
57 g in 1 TUBE (82729-006-01)

Annotations

UNII (FDA Substance ID)

N20HL7Q941

CAMPHOR (NATURAL)

RxCUI 1298738

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "N20HL7Q941",
    "rxcui": "1298738",
    "inchikey": "DSSYKIVIOFKYAU-XCBNKYQSSA-N",
    "display_name": "CAMPHOR (NATURAL)",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "TOPICAL",
  "spl_meta": {
    "52d4b1c1-7431-4f8c-e063-6294a90ad482": {
      "match": "brand_token",
      "title": "ULTRA VIOLETTE VELVET SCREEN BLURRING MINERAL SKINSCREEN BROAD SPECTRUM SPF 40 (ZINC OXIDE) CREAM [GRACE AND FIRE USA INC.]",
      "spl_version": "1",
      "published_date": "2026-05-29"
    }
  },
  "productid": "82729-006_4db9acb8-4f1d-ca46-e063-6394a90aed52",
  "productndc": "82729-006",
  "dosage_form": "CREAM",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "CAMPHOR (NATURAL); LEVOMENTHOL; METHYL SALICYLATE",
  "proprietary_name": "Ultra Strength Topical Pain Relief Cream",
  "active_ingred_unit": "mg/g; mg/g; mg/g",
  "application_number": "M017",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "Camphor, Menthol, Methyl Salicylate",
  "start_marketing_date": "20260331",
  "active_numerator_strength": "40; 100; 300"
}

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