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United States · US · US:29784-601_252a0dfe-c0dc-640c-e063-6394a90a999b
Profoot Pain Relief Patches
SPL
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerProfoot, Inc.
CountryUS (United States)
ATC code—
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc1129784601011 KIT in 1 KIT (29784-601-01) * 1 PATCH in 1 KIT / .36 g in 1 PATCH (29784-121-36) * 2 PATCH in 1 KIT / 1.3 g in 1 PATCH (29784-122-36)
Annotations
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"route": null,
"spl_meta": {
"cc011b79-2761-40f7-8142-88f8e30a179a": {
"match": "brand_token",
"title": "PROFOOT PAIN RELIEF PATCHES (CAMPHOR, MENTHOL, METHYL SALICYLATE) KIT [ROOFTOP CONSUMER HEALTH, INC.]",
"spl_version": "19",
"published_date": "2024-10-25"
}
},
"productid": "29784-601_252a0dfe-c0dc-640c-e063-6394a90a999b",
"productndc": "29784-601",
"dosage_form": "KIT",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": null,
"proprietary_name": "Profoot Pain Relief Patches",
"active_ingred_unit": null,
"application_number": "M017",
"marketing_category": "OTC MONOGRAPH DRUG",
"nonproprietary_name": "CAMPHOR, MENTHOL, METHYL SALICYLATE",
"start_marketing_date": "20231012",
"active_numerator_strength": null
}Access this data programmatically
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