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United States · US · US:61577-3242_364d60f1-80e4-1ee1-e063-6394a90ab590
RE-LEVE
SPL
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerSOMBRA COSMETICS INC.
CountryUS (United States)
ATC code—
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 2
- ndc116157732424113.6 g in 1 JAR (61577-3242-4)
- ndc116157732425113.6 g in 1 TUBE (61577-3242-5)
Annotations
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"route": "TOPICAL",
"spl_meta": {
"b4b39d79-0439-41e7-adca-e5ccb8f44e40": {
"match": "brand_token",
"title": "RE-LEVE (MENTHOL) GEL [SOMBRA COSMETICS INC.]",
"spl_version": "6",
"published_date": "2025-06-02"
}
},
"productid": "61577-3242_364d60f1-80e4-1ee1-e063-6394a90ab590",
"productndc": "61577-3242",
"dosage_form": "GEL",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "MENTHOL",
"proprietary_name": "RE-LEVE",
"active_ingred_unit": "g/g",
"application_number": "M017",
"marketing_category": "OTC MONOGRAPH DRUG",
"nonproprietary_name": "MENTHOL",
"start_marketing_date": "20161005",
"active_numerator_strength": ".06"
}Access this data programmatically
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