ULTRA RELIEF

UNIISPL

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

Identification

ManufacturerCHEMCO CORPORATION

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
4928357804
113 g in 1 BOTTLE, PUMP (49283-578-04)

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": {
    "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": "49283-578_48e9bcf4-0751-7b3f-e063-6294a90ac649",
  "productndc": "49283-578",
  "dosage_form": "GEL",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "CAMPHOR (SYNTHETIC); MENTHOL",
  "proprietary_name": "ULTRA RELIEF",
  "active_ingred_unit": "g/100g; g/100g",
  "application_number": "M017",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "MENTHOL, CAMPHOR",
  "start_marketing_date": "20260115",
  "active_numerator_strength": "3; 6"
}

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