DAYDREAM Broad Spectrum Sunscreen SPF 40

UNIISPL

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

Identification

ManufacturerDrmtlgy, LLC

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
8328600101
1 JAR in 1 CARTON (83286-001-01) / 50 mL in 1 JAR

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": {
    "36bfd963-d123-0d25-e063-6294a90aa827": {
      "match": "brand_token",
      "title": "DAYDREAM BEYOND SCREEN (ZINC OXIDE) CREAM [ULTRAVIOLET SKINCARE LLC]",
      "spl_version": "2",
      "published_date": "2025-12-17"
    }
  },
  "productid": "83286-001_7e379b89-a82f-4101-93d1-0e7ffd1e4b54",
  "productndc": "83286-001",
  "dosage_form": "CREAM",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "ZINC OXIDE",
  "proprietary_name": "DAYDREAM Broad Spectrum Sunscreen SPF 40",
  "active_ingred_unit": "g/100mL",
  "application_number": "M020",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "Zinc Oxide",
  "start_marketing_date": "20230221",
  "active_numerator_strength": "17"
}

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