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United States Β· US Β· US:59316-207_51e06d5e-11fe-5814-e063-6294a90a2736
Biofreeze Overnight Roll-on
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
- ndc11593162071474 mL in 1 BOTTLE (59316-207-14)
Annotations
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"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": "59316-207_51e06d5e-11fe-5814-e063-6294a90a2736",
"productndc": "59316-207",
"dosage_form": "GEL",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "MENTHOL",
"proprietary_name": "Biofreeze Overnight Roll-on",
"active_ingred_unit": "mg/mL",
"application_number": "M017",
"marketing_category": "OTC MONOGRAPH DRUG",
"nonproprietary_name": "Menthol",
"start_marketing_date": "20230316",
"active_numerator_strength": "40"
}Access this data programmatically
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