Overnight Cold Therapy Pain Relief

UNIISPL

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

Identification

ManufacturerWalgreen Co.

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 2

ndc11
0363035503
89 mL in 1 TUBE (0363-0355-03)
ndc11
0363035525
74 mL in 1 BOTTLE, WITH APPLICATOR (0363-0355-25)

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": {
    "2c6c4737-dff3-6382-e063-6294a90a412c": {
      "match": "brand_token",
      "title": "OVERNIGHT RELIEF GEL-PATCH (MENTHOL) PATCH [SHANGHAI CHUANGSHI MEDICAL TECHNOLOGY (GROUP) CO., LTD.]",
      "spl_version": "2",
      "published_date": "2026-05-20"
    }
  },
  "productid": "0363-0355_5f845434-d8db-4bfa-8fc0-8a9b9205f194",
  "productndc": "0363-0355",
  "dosage_form": "GEL",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "MENTHOL, UNSPECIFIED FORM",
  "proprietary_name": "Overnight 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": "20231204",
  "active_numerator_strength": "36"
}

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