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United States Β· US Β· US:59316-002_51b58d16-badb-06b8-e063-6294a90a94ea
Biofreeze Foot Pain Relief Set
SPL
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerReckitt Benckiser LLC
CountryUS (United States)
ATC codeβ
Dispensingβ
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs Β· 1
- ndc1159316002101 KIT in 1 KIT (59316-002-10) * 85 g in 1 TUBE (59316-001-10)
Annotations
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"route": null,
"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": "59316-002_51b58d16-badb-06b8-e063-6294a90a94ea",
"productndc": "59316-002",
"dosage_form": "KIT",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": null,
"proprietary_name": "Biofreeze Foot Pain Relief Set",
"active_ingred_unit": null,
"application_number": "M017",
"marketing_category": "OTC MONOGRAPH DRUG",
"nonproprietary_name": "MENTHOL",
"start_marketing_date": "20210312",
"active_numerator_strength": null
}Access this data programmatically
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