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United States · US · US:84779-115_3a017a63-4a10-f57e-e063-6394a90ab7bb
Amarte ULTRA VEIL Daily
SPLATC D02BA
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerAmarte USA LLC
CountryUS (United States)
ATC codeD02BA
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 2
- ndc1184779115051 BOTTLE in 1 BOX (84779-115-05) / 5 mL in 1 BOTTLE
- ndc1184779115701 BOTTLE in 1 BOX (84779-115-70) / 70 mL in 1 BOTTLE
Annotations
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"route": "TOPICAL",
"spl_meta": {
"39e87950-4103-c2eb-e063-6394a90a0552": {
"match": "brand_token",
"title": "AMARTE ULTRA VEIL BB FAIR (SUNSCREEN) LOTION AMARTE ULTRA VEIL BB NATURAL (SUNSCREEN) LOTION AMARTE ULTRA VEIL BB TAN (SUNSCREEN) LOTION [AMARTE USA LLC]",
"spl_version": "2",
"published_date": "2025-07-17"
}
},
"productid": "84779-115_3a017a63-4a10-f57e-e063-6394a90ab7bb",
"productndc": "84779-115",
"dosage_form": "LOTION",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "ETHYLHEXYL METHOXYCINNAMATE; ETHYLHEXYL SALICYLATE; TITANIUM DIOXIDE; ZINC OXIDE",
"proprietary_name": "Amarte ULTRA VEIL Daily",
"active_ingred_unit": "mg/mL; mg/mL; mg/mL; mg/mL",
"application_number": "M020",
"marketing_category": "OTC MONOGRAPH DRUG",
"nonproprietary_name": "Sunscreen",
"start_marketing_date": "20250715",
"active_numerator_strength": "40; 40; 50; 30"
}Related drugs
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