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United States Β· US Β· US:85449-208_460097a6-d949-13cb-e063-6394a90ab585
Superscreen Daytime Mineral Sunscreen
UNIISPL
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerMCRAE MD MEDICAL LASER CENTER, A TEXAS PROFESSIONAL LIMITED LIABILITY COMPANY
CountryUS (United States)
ATC codeβ
Dispensingβ
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs Β· 1
- ndc11854492085050 g in 1 BOTTLE, PUMP (85449-208-50)
Annotations
UNII (FDA Substance ID)
SOI2LOH54Z
ZINC OXIDE
RxCUI 11423
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "SOI2LOH54Z",
"rxcui": "11423",
"inchikey": "RNWHGQJWIACOKP-UHFFFAOYSA-N",
"display_name": "ZINC OXIDE",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "TOPICAL",
"spl_meta": {
"ff0e4e97-8f01-bd36-e053-6394a90a47ae": {
"match": "brand_token",
"title": "SUPERSCREEN HYDRATING DAILY CREAM SPF 40 (AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE) CREAM [SUPERGOOP, LLC]",
"spl_version": "2",
"published_date": "2026-01-12"
}
},
"productid": "85449-208_460097a6-d949-13cb-e063-6394a90ab585",
"productndc": "85449-208",
"dosage_form": "CREAM",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "ZINC OXIDE",
"proprietary_name": "Superscreen Daytime Mineral Sunscreen",
"active_ingred_unit": "mg/g",
"application_number": "M020",
"marketing_category": "OTC MONOGRAPH DRUG",
"nonproprietary_name": "Zinc Oxide",
"start_marketing_date": "20231108",
"active_numerator_strength": "160"
}Access this data programmatically
Query Superscreen Daytime Mineral Sunscreen and 610,000+ other drug records through a single REST API β with a last_synced_at provenance stamp on every response. Free tier includes 100 requests/day.