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United States · US · US:84803-111_47b7dab4-2800-9cda-e063-6394a90a24da
ULTRA VIOLETTE SPF ON THE GLOW
SPL
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerGrace And Fire USA Inc.
CountryUS (United States)
ATC code—
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc1184803111011 KIT in 1 KIT (84803-111-01) * 30 mL in 1 BOTTLE, SPRAY (84803-101-30) * 15 g in 1 TUBE (84803-104-02)
Annotations
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"route": "TOPICAL",
"spl_meta": {
"52d4b1c1-7431-4f8c-e063-6294a90ad482": {
"match": "brand_token",
"title": "ULTRA VIOLETTE VELVET SCREEN BLURRING MINERAL SKINSCREEN BROAD SPECTRUM SPF 40 (ZINC OXIDE) CREAM [GRACE AND FIRE USA INC.]",
"spl_version": "1",
"published_date": "2026-05-29"
}
},
"productid": "84803-111_47b7dab4-2800-9cda-e063-6394a90a24da",
"productndc": "84803-111",
"dosage_form": "KIT",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": null,
"proprietary_name": "ULTRA VIOLETTE SPF ON THE GLOW",
"active_ingred_unit": null,
"application_number": "M020",
"marketing_category": "OTC MONOGRAPH DRUG",
"nonproprietary_name": "SPF 50",
"start_marketing_date": "20241129",
"active_numerator_strength": null
}Access this data programmatically
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