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United States · US · US:0363-0356_f2ea3545-6938-4a13-8969-32f38f3d9fff

Cold Therapy Pain Relief

UNIISPL

Last synced from FDA National Drug Code directory (United States) on

Identification

ManufacturerWalgreen Co.
CountryUS (United States)
ATC code
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 2

  • ndc11
    0363035603
    89 mL in 1 TUBE (0363-0356-03)
  • ndc11
    0363035625
    74 mL in 1 BOTTLE, WITH APPLICATOR (0363-0356-25)

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": {
    "adb658c8-db8d-4db6-80c8-e0f2de88a2de": {
      "match": "brand_token",
      "title": "COLD AND FLU NIGHTTIME (ACETAMINOPHEN, DEXTROMETHORPHAN HBR, TRIPROLIDINE HCL) SOLUTION [WALMART INC.]",
      "spl_version": "7",
      "published_date": "2026-05-28"
    }
  },
  "productid": "0363-0356_f2ea3545-6938-4a13-8969-32f38f3d9fff",
  "productndc": "0363-0356",
  "dosage_form": "GEL",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "MENTHOL, UNSPECIFIED FORM",
  "proprietary_name": "Cold Therapy Pain Relief",
  "active_ingred_unit": "mg/mL",
  "application_number": "M017",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "Menthol, unspecified form",
  "start_marketing_date": "20240401",
  "active_numerator_strength": "36"
}

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