Ultra-Strength Pain Relief

UNIISPL

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

Identification

ManufacturerTARGET CORPORATION

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
8244231101
1 JAR in 1 CARTON (82442-311-01) / 18 g in 1 JAR

Annotations

UNII (FDA Substance ID)

5TJD82A1ET

CAMPHOR (SYNTHETIC)

RxCUI 1371994

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "5TJD82A1ET",
    "rxcui": "1371994",
    "inchikey": "DSSYKIVIOFKYAU-XCBNKYQSSA-N;DSSYKIVIOFKYAU-OIBJUYFYSA-N",
    "display_name": "CAMPHOR (SYNTHETIC)",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "TOPICAL",
  "spl_meta": {
    "159c5a84-bf68-41dd-a2d3-bc2402037244": {
      "match": "brand_token",
      "title": "ULTRA-STRENGTH PAIN RELIEF ANALGESIC (CAMPHOR (SYNTHETIC) AND MENTHOL, UNSPECIFIED FORM) OINTMENT [TARGET CORPORATION]",
      "spl_version": "2",
      "published_date": "2025-11-25"
    }
  },
  "productid": "82442-311_9029fd41-a09a-4651-828c-5b033dd14c9a",
  "productndc": "82442-311",
  "dosage_form": "OINTMENT",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "CAMPHOR (SYNTHETIC); MENTHOL, UNSPECIFIED FORM",
  "proprietary_name": "Ultra-Strength Pain Relief",
  "active_ingred_unit": "mg/g; mg/g",
  "application_number": "M017",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "CAMPHOR (SYNTHETIC) and MENTHOL, UNSPECIFIED FORM",
  "start_marketing_date": "20241014",
  "active_numerator_strength": "110; 110"
}

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