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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

  • ndc11
    7122008708
    1 TUBE in 1 BOX (71220-087-08) / 50 mL in 1 TUBE
  • ndc11
    7122008741
    1 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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Innisfree Daily UV Defense Mineral Sunscreen (US) β€” Drug Database