CORE RELIEF

UNIISPL

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

Identification

ManufacturerCopper Joint, LLC

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 2

ndc11
8717905302
59 mL in 1 JAR (87179-053-02)
ndc11
8717905303
10 mL in 1 PACKET (87179-053-03)

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": {
    "f76dfeca-4e86-0b5d-e053-6294a90a29b9": {
      "match": "brand_token",
      "title": "CORE VALUES EYE DROPS ADVANCED RELIEF (DEXTRAN 70, POLYETHYLENE GLYCOL 400, POVIDONE, TETRAHYDROZOLINE HYDROCHLORIDE) SOLUTION/ DROPS [LIBERTY PROCUREMENT CO., INC.]",
      "spl_version": "3",
      "published_date": "2026-01-02"
    }
  },
  "productid": "87179-053_42d18abb-8f40-a079-e063-6294a90a18ee",
  "productndc": "87179-053",
  "dosage_form": "CREAM",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "CAMPHOR (SYNTHETIC); MENTHOL",
  "proprietary_name": "CORE RELIEF",
  "active_ingred_unit": "g/100mL; g/100mL",
  "application_number": "M017",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "Camphor, Menthol",
  "start_marketing_date": "20251110",
  "active_numerator_strength": "3; 5"
}

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