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United States · US · US:55715-008_315525bd-c7a7-77aa-e063-6394a90a89bf
Zpol ULTRA
SPL
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerLaboratorios Zepol S.A.
CountryUS (United States)
ATC code—
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 3
- ndc11557150080129 g in 1 BOTTLE, PLASTIC (55715-008-01)
- ndc11557150080259 g in 1 BOTTLE, PLASTIC (55715-008-02)
- ndc115571500803119 g in 1 BOTTLE, PLASTIC (55715-008-03)
Annotations
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"route": "TOPICAL",
"spl_meta": {
"1a1433a6-8d04-96df-e063-6394a90a987b": {
"match": "brand_token",
"title": "ZPOL ULTRA (MENTHOL, METHYL SALICYLATE) CREAM [LABORATORIOS ZEPOL S.A.]",
"spl_version": "3",
"published_date": "2025-04-03"
}
},
"productid": "55715-008_315525bd-c7a7-77aa-e063-6394a90a89bf",
"productndc": "55715-008",
"dosage_form": "CREAM",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "MENTHOL; METHYL SALICYLATE",
"proprietary_name": "Zpol ULTRA",
"active_ingred_unit": "g/100g; g/100g",
"application_number": "M017",
"marketing_category": "OTC MONOGRAPH DRUG",
"nonproprietary_name": "MENTHOL, METHYL SALICYLATE",
"start_marketing_date": "20250401",
"active_numerator_strength": "2.84; 18.24"
}Access this data programmatically
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