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United States · US · US:85586-001_341c720c-38dd-4cba-e063-6394a90a66a8
LAPCOS DAILY SUNSCREEN SPF 50
SPL
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerLAP USA, INC.
CountryUS (United States)
ATC code—
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc1185586001021 TUBE in 1 BOX (85586-001-02) / 50 g in 1 TUBE (85586-001-01)
Annotations
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"route": "TOPICAL",
"spl_meta": {
"337c3528-5739-6b4a-e063-6294a90a3cb4": {
"match": "brand_token",
"title": "LAPCOS DAILY SUNSCREEN SPF 50 (SUNSCREEN) CREAM [LAP USA, INC.]",
"spl_version": "2",
"published_date": "2025-05-05"
}
},
"productid": "85586-001_341c720c-38dd-4cba-e063-6394a90a66a8",
"productndc": "85586-001",
"dosage_form": "CREAM",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "ETHYLHEXYL SALICYLATE; HOMOSALATE; OCTOCRYLENE; ZINC OXIDE",
"proprietary_name": "LAPCOS DAILY SUNSCREEN SPF 50",
"active_ingred_unit": "g/100g; g/100g; g/100g; g/100g",
"application_number": "M020",
"marketing_category": "OTC MONOGRAPH DRUG",
"nonproprietary_name": "sunscreen",
"start_marketing_date": "20250423",
"active_numerator_strength": "4.5; 6; 5; 10.3"
}Access this data programmatically
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