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United States · US · US:70015-665_51a0db5e-9e53-71c2-e063-6394a90a1bb2
Instaflex Pain Relief Cream
SPL
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerHealthy Directions, LLC
CountryUS (United States)
ATC code—
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 3
- ndc1170015665011 TUBE in 1 CARTON (70015-665-01) / 28 g in 1 TUBE
- ndc1170015665021 TUBE in 1 CARTON (70015-665-02) / 57 g in 1 TUBE
- ndc1170015665041 TUBE in 1 CARTON (70015-665-04) / 113 g in 1 TUBE
Annotations
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"route": "TOPICAL",
"spl_meta": {
"d058c64d-0e4f-45aa-8f52-804961b562e3": {
"match": "brand_token",
"title": "INSTAFLEX EXTRA STRENGTH PAIN RELIEF CREAM (MENTHOL, METHYL SALICYLATE) CREAM [HEALTHY DIRECTIONS, LLC]",
"spl_version": "2",
"published_date": "2026-05-13"
}
},
"productid": "70015-665_51a0db5e-9e53-71c2-e063-6394a90a1bb2",
"productndc": "70015-665",
"dosage_form": "CREAM",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "MENTHOL",
"proprietary_name": "Instaflex Pain Relief Cream",
"active_ingred_unit": "mg/g",
"application_number": "M017",
"marketing_category": "OTC MONOGRAPH DRUG",
"nonproprietary_name": "Menthol",
"start_marketing_date": "20190101",
"active_numerator_strength": "12.5"
}Access this data programmatically
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