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United States · US · US:85448-003_4ed974b8-6c12-08e0-e063-6294a90a7713
Ultra Sunscreen
UNIISPLATC D02BA
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerJiangsu Senwo Medical Technology Co., Ltd.
CountryUS (United States)
ATC codeD02BA
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc118544800301473 mL in 1 BOTTLE (85448-003-01)
Annotations
UNII (FDA Substance ID)
4Y5P7MUD51
OCTINOXATE
RxCUI 13369
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "4Y5P7MUD51",
"rxcui": "13369",
"inchikey": "YBGZDTIWKVFICR-JLHYYAGUSA-N",
"display_name": "OCTINOXATE",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"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": "85448-003_4ed974b8-6c12-08e0-e063-6294a90a7713",
"productndc": "85448-003",
"dosage_form": "EMULSION",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "OCTINOXATE; OCTISALATE; TITANIUM DIOXIDE",
"proprietary_name": "Ultra Sunscreen",
"active_ingred_unit": "g/mL; g/mL; g/mL",
"application_number": "M020",
"marketing_category": "OTC MONOGRAPH DRUG",
"nonproprietary_name": "Octinoxate, Octisalate, Titanium Dioxide",
"start_marketing_date": "20260407",
"active_numerator_strength": ".09; .035; .027"
}Related drugs
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