Surface Sun SPF 50 Mineral

UNIISPL

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

Identification

ManufacturerSurface Products Corp

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
7234411003
88 mL in 1 TUBE (72344-110-03)

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": {
    "bdab8c55-1624-49c5-8357-27f68b86f7c7": {
      "match": "brand_token",
      "title": "SURFACE X CUTIE PALS HAND SANITIZER CARAMEL LATTE (ALCOHOL) SPRAY [I WORLD, LLC]",
      "spl_version": "1",
      "published_date": "2026-05-20"
    }
  },
  "productid": "72344-110_510367d3-8ba2-ca59-e063-6394a90a2ac8",
  "productndc": "72344-110",
  "dosage_form": "LOTION",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "ZINC OXIDE",
  "proprietary_name": "Surface Sun SPF 50 Mineral",
  "active_ingred_unit": "g/100mL",
  "application_number": "M020",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "Zinc Oxide",
  "start_marketing_date": "20251201",
  "active_numerator_strength": "20"
}

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