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United States · US · US:32472-102_46a6f042-1931-0688-e063-6294a90ae162
Premieres Pain
SPL
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerPremiere Enterprises
CountryUS (United States)
ATC code—
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc11324721020129.5 mL in 1 BOTTLE (32472-102-01)
Annotations
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"route": "TOPICAL",
"spl_meta": {
"128bd1e7-e961-416c-933b-fbd146e3d386": {
"match": "brand_token",
"title": "PREMIERES PAIN (MENTHOL) SPRAY [PREMIERE ENTERPRISES]",
"spl_version": "6",
"published_date": "2025-12-25"
}
},
"productid": "32472-102_46a6f042-1931-0688-e063-6294a90ae162",
"productndc": "32472-102",
"dosage_form": "SPRAY",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "MENTHOL",
"proprietary_name": "Premieres Pain",
"active_ingred_unit": "g/100mL",
"application_number": "M017",
"marketing_category": "OTC MONOGRAPH DRUG",
"nonproprietary_name": "menthol",
"start_marketing_date": "20110307",
"active_numerator_strength": "7"
}Access this data programmatically
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