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United States · US · US:10742-8169_29791c3e-3ae3-2db5-e063-6394a90a2075
Mentholatum Pain Relieving
UNIISPL
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerThe Mentholatum Company
CountryUS (United States)
ATC code—
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 2
- ndc1110742816911 BOTTLE in 1 CARTON (10742-8169-1) / 100 mL in 1 BOTTLE
- ndc1110742816921 BOTTLE in 1 CARTON (10742-8169-2) / 75 mL in 1 BOTTLE
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": {
"37f2c3a6-7790-c8ec-e063-6294a90ace22": {
"match": "brand_token",
"title": "MENTHOLATUM NATURAL ICE CHERRY, SPF 15 CHERRY (DIMETHICONE, OCTINOXATE, OCTISALATE) STICK [THE MENTHOLATUM COMPANY]",
"spl_version": "2",
"published_date": "2026-03-26"
}
},
"productid": "10742-8169_29791c3e-3ae3-2db5-e063-6394a90a2075",
"productndc": "10742-8169",
"dosage_form": "LOTION",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "MENTHOL, UNSPECIFIED FORM; METHYL SALICYLATE",
"proprietary_name": "Mentholatum Pain Relieving",
"active_ingred_unit": "mg/mL; mg/mL",
"application_number": "M017",
"marketing_category": "OTC MONOGRAPH DRUG",
"nonproprietary_name": "menthol, methyl salicylate",
"start_marketing_date": "20181101",
"active_numerator_strength": "60; 200"
}Access this data programmatically
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