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United States · US · US:59316-103_51b597cc-8068-e160-e063-6394a90ac1be
Biofreeze Colorless
UNIISPL
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerReckitt Benckiser LLC
CountryUS (United States)
ATC code—
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 3
- ndc11593161031289 mL in 1 BOTTLE (59316-103-12)
- ndc115931610320118 mL in 1 BOTTLE (59316-103-20)
- ndc115931610340946 mL in 1 BOTTLE (59316-103-40)
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": {
"71a36691-9d9e-479d-bfdc-6f6b192ad2d0": {
"match": "brand_token",
"title": "BIOFREEZE MENTHOL (MENTHOL, UNSPECIFIED FORM) PATCH [RECKITT BENCKISER LLC]",
"spl_version": "4",
"published_date": "2026-05-28"
}
},
"productid": "59316-103_51b597cc-8068-e160-e063-6394a90ac1be",
"productndc": "59316-103",
"dosage_form": "GEL",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "MENTHOL, UNSPECIFIED FORM",
"proprietary_name": "Biofreeze Colorless",
"active_ingred_unit": "mg/mL",
"application_number": "M017",
"marketing_category": "OTC MONOGRAPH DRUG",
"nonproprietary_name": "MENTHOL",
"start_marketing_date": "20120103",
"active_numerator_strength": "40"
}Access this data programmatically
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