Illuminating Daily SPF 40 Lightly Tinted

UNIISPL

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

Identification

ManufacturerFace 5, LLC

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
8530220815
1.5 g in 1 PACKET (85302-208-15)

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": "85302-208_4577dd11-5f9b-f302-e063-6294a90ae1d3",
  "productndc": "85302-208",
  "dosage_form": "CREAM",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "ZINC OXIDE",
  "proprietary_name": "Illuminating Daily SPF 40 Lightly Tinted",
  "active_ingred_unit": "mg/g",
  "application_number": "M020",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "Zinc Oxide",
  "start_marketing_date": "20221123",
  "active_numerator_strength": "160"
}

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