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United States · US · US:83574-413_2bbc8ed1-176c-27a5-e063-6394a90a38ee
K19 RELIEF
SPL
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerK19 LLC
CountryUS (United States)
ATC code—
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc118357441300295 mL in 1 BOTTLE, SPRAY (83574-413-00)
Annotations
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"route": "TOPICAL",
"spl_meta": {
"e2e1ca96-1ae8-4c99-b8de-ce26754292f9": {
"match": "brand_token",
"title": "K19 RELIEF (MENTHOL) LIQUID [K19 LLC]",
"spl_version": "3",
"published_date": "2025-01-16"
}
},
"productid": "83574-413_2bbc8ed1-176c-27a5-e063-6394a90a38ee",
"productndc": "83574-413",
"dosage_form": "LIQUID",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "MENTHOL",
"proprietary_name": "K19 RELIEF",
"active_ingred_unit": "mg/mL",
"application_number": "M017",
"marketing_category": "OTC MONOGRAPH DRUG",
"nonproprietary_name": "MENTHOL",
"start_marketing_date": "20230710",
"active_numerator_strength": "12.5"
}Access this data programmatically
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