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United States · US · US:85302-226_4577d963-6780-f387-e063-6294a90af53d
Illuminating Daily SPF40 Non-Tinted
UNIISPL
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerFace 5, LLC
CountryUS (United States)
ATC code—
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc11853022265050 g in 1 BOTTLE, PUMP (85302-226-50)
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": {
"35bb4d67-373f-f60c-e063-6394a90a974d": {
"match": "brand_token",
"title": "ILLUMINATING MINERAL MOUSSE (TITANIUM DIOXIDE, ZINC OXIDE) AEROSOL, FOAM [NEXTEX CORPORATION]",
"spl_version": "2",
"published_date": "2025-12-15"
}
},
"productid": "85302-226_4577d963-6780-f387-e063-6294a90af53d",
"productndc": "85302-226",
"dosage_form": "CREAM",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "ZINC OXIDE",
"proprietary_name": "Illuminating Daily SPF40 Non-Tinted",
"active_ingred_unit": "mg/g",
"application_number": "M020",
"marketing_category": "OTC MONOGRAPH DRUG",
"nonproprietary_name": "Zinc Oxide",
"start_marketing_date": "20240417",
"active_numerator_strength": "160"
}Access this data programmatically
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