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United States Β· US Β· US:71220-087_2619fd9d-f9e1-18c1-e063-6394a90aa334
Innisfree Daily UV Defense Mineral Sunscreen
UNIISPL
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerInnisfree Corporation
CountryUS (United States)
ATC codeβ
Dispensingβ
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs Β· 2
- ndc1171220087081 TUBE in 1 BOX (71220-087-08) / 50 mL in 1 TUBE
- ndc1171220087411 TUBE in 1 BOX (71220-087-41) / 10 mL in 1 TUBE
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": {
"0e9b6697-28a3-f69f-e063-6394a90a9d11": {
"match": "brand_token",
"title": "INNISFREE DAILY UV DEFENSE SUNSCREEN (AVOBENZONE, HOMOSALATE, AND OCTISALATE LOTION) LOTION [INNISFREE CORPORATION]",
"spl_version": "6",
"published_date": "2025-11-21"
}
},
"productid": "71220-087_2619fd9d-f9e1-18c1-e063-6394a90aa334",
"productndc": "71220-087",
"dosage_form": "LOTION",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "ZINC OXIDE",
"proprietary_name": "Innisfree Daily UV Defense Mineral Sunscreen",
"active_ingred_unit": "g/50mL",
"application_number": "M020",
"marketing_category": "OTC MONOGRAPH DRUG",
"nonproprietary_name": "Zinc Oxide Lotion",
"start_marketing_date": "20240201",
"active_numerator_strength": "8"
}Access this data programmatically
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