Daily Face Broad Spectrum

UNIISPL

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

Identification

ManufacturerHarry's, Inc.

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
7053300150
1 BOTTLE in 1 CARTON (70533-001-50) / 50 mL in 1 BOTTLE

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": {
    "52f818f4-8485-b228-e063-6294a90a9fe3": {
      "match": "brand_token",
      "title": "DAILY MINERAL SUNSCREEN 20% ZINC OXIDE (ZINC OXIDE) CREAM [INTEGRATIVE AESTHETICS BOSTON, LLC]",
      "spl_version": "1",
      "published_date": "2026-06-01"
    }
  },
  "productid": "70533-001_2fab0ad2-7453-53fc-e054-00144ff8d46c",
  "productndc": "70533-001",
  "dosage_form": "LOTION",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "ZINC OXIDE",
  "proprietary_name": "Daily Face Broad Spectrum",
  "active_ingred_unit": "mg/mL",
  "application_number": "part352",
  "marketing_category": "OTC MONOGRAPH NOT FINAL",
  "nonproprietary_name": "ZINC OXIDE",
  "start_marketing_date": "20160401",
  "active_numerator_strength": "66"
}

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