Kiss My Face Purely Mineral Daily 50 Sunscreen SPF 50

UNIISPL

Last synced from FDA National Drug Code directory (United States) on June 3, 2026

Identification

ManufacturerWindmill Health Products, LLC

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
7415490300
118 mL in 1 BOTTLE (74154-903-00)

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": {
    "ebfb149c-0371-4492-b03a-5fdcb7821753": {
      "match": "brand_token",
      "title": "KISS MY FACE PURELY MINERAL DAILY 50 SUNSCREEN SPF 50 (ZINC OXIDE) LOTION [WINDMILL HEALTH PRODUCTS, LLC]",
      "spl_version": "1",
      "published_date": "2026-02-26"
    }
  },
  "productid": "74154-903_4ba3d83b-0005-b5de-e063-6294a90acc39",
  "productndc": "74154-903",
  "dosage_form": "LOTION",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "ZINC OXIDE",
  "proprietary_name": "Kiss My Face Purely Mineral Daily 50 Sunscreen SPF 50",
  "active_ingred_unit": "mg/mL",
  "application_number": "M020",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "ZINC OXIDE",
  "start_marketing_date": "20260204",
  "active_numerator_strength": "175"
}

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