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United States · US · US:58559-001_48617c36-0ba4-cc34-e063-6394a90a0f20
Relief Pain Relieving Cream
SPL
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerCorganics, LP
CountryUS (United States)
ATC code—
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 5
- ndc1158559001015 g in 1 BLISTER PACK (58559-001-01)
- ndc11585590010282 g in 1 BOTTLE, WITH APPLICATOR (58559-001-02)
- ndc115855900103115 g in 1 TUBE (58559-001-03)
- ndc115855900104450 g in 1 BOTTLE, PUMP (58559-001-04)
- ndc1158559001053600 g in 1 BOTTLE, PUMP (58559-001-05)
Annotations
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"route": "TOPICAL",
"spl_meta": {
"49e6f0ef-78fb-26fe-e063-6294a90a6655": {
"match": "brand_token",
"title": "RELIEF FLEX (MENTHOL) PATCH [BEONE CO., LTD.]",
"spl_version": "1",
"published_date": "2026-02-04"
}
},
"productid": "58559-001_48617c36-0ba4-cc34-e063-6394a90a0f20",
"productndc": "58559-001",
"dosage_form": "CREAM",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "MENTHOL",
"proprietary_name": "Relief Pain Relieving Cream",
"active_ingred_unit": "g/100g",
"application_number": "M017",
"marketing_category": "OTC MONOGRAPH DRUG",
"nonproprietary_name": "MENTHOL",
"start_marketing_date": "20040522",
"active_numerator_strength": "2.5"
}Access this data programmatically
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