Daily SPF Facial SunscreenLotion Broad Spectrum SPF 32

UNIISPL

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

Identification

ManufacturerOnekind.25

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
7935620120
1 TUBE in 1 CARTON (79356-201-20) / 48 g in 1 TUBE (79356-201-10)

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": "79356-201_45fef171-4358-07b4-e063-6394a90a208f",
  "productndc": "79356-201",
  "dosage_form": "CREAM",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "ZINC OXIDE",
  "proprietary_name": "Daily SPF Facial SunscreenLotion Broad Spectrum SPF 32",
  "active_ingred_unit": "mg/g",
  "application_number": "M020",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "Zinc Oxide",
  "start_marketing_date": "20201103",
  "active_numerator_strength": "210"
}

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