ARCTIC RELIEF

UNIISPL

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

Identification

ManufacturerSTRATUS PHARMACEUTICALS INC

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
5898061540
1 TUBE in 1 BOX (58980-615-40) / 113.4 g in 1 TUBE

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": {
    "402df5c1-b8cb-17a2-e054-00144ff8d46c": {
      "match": "brand_token",
      "title": "ARCTIC HEAT (MENTHOL, METHYL SALICYLATE) CREAM [RENU LABORATORIES, LLC]",
      "spl_version": "8",
      "published_date": "2025-09-15"
    }
  },
  "productid": "58980-615_db73c60c-1ff8-4b16-a467-6f0b8727f1d6",
  "productndc": "58980-615",
  "dosage_form": "GEL",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "MENTHOL, UNSPECIFIED FORM",
  "proprietary_name": "ARCTIC RELIEF",
  "active_ingred_unit": "g/113.4g",
  "application_number": "M017",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "MENTHOL, UNSPECIFIED FORM",
  "start_marketing_date": "20170915",
  "active_numerator_strength": "3.969"
}

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