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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
- ndc11036303560389 mL in 1 TUBE (0363-0356-03)
- ndc11036303562574 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"
}Access this data programmatically
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