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United States · US · US:85350-039_40ffa941-e0b5-3f35-e063-6394a90a9d6f
Doloflex Pain Relief
SPL
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerUnited Health & Beauty Corp
CountryUS (United States)
ATC code—
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 2
- ndc118535003910300 g in 1 JAR (85350-039-10)
- ndc118535003911300 g in 1 JAR (85350-039-11)
Annotations
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"route": "TOPICAL",
"spl_meta": {
"32a830cc-04d3-102e-e063-6294a90a1cad": {
"match": "brand_token",
"title": "DOLOFLEX PAIN RELIEF (MENTHOL, METHYL SALICYLATE) GEL [UNITED HEALTH & BEAUTY CORP]",
"spl_version": "2",
"published_date": "2025-11-17"
}
},
"productid": "85350-039_40ffa941-e0b5-3f35-e063-6394a90a9d6f",
"productndc": "85350-039",
"dosage_form": "GEL",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "MENTHOL; METHYL SALICYLATE",
"proprietary_name": "Doloflex Pain Relief",
"active_ingred_unit": "g/100g; g/100g",
"application_number": "M017",
"marketing_category": "OTC MONOGRAPH DRUG",
"nonproprietary_name": "Menthol, Methyl Salicylate",
"start_marketing_date": "20250317",
"active_numerator_strength": "2; 10"
}Access this data programmatically
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