Non Tinted Moisturizing Mineral Sunscreen

UNIISPL

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

Identification

ManufacturerEDIT EUROSPA, LLC

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
8564220504
113 g in 1 BOTTLE, PUMP (85642-205-04)

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": {
    "600855d4-36c4-41d6-a7aa-d0f373aad57e": {
      "match": "brand_token",
      "title": "NON IODINE BARRIER DIP (IODINE) SOLUTION [SURPASS CHEMICAL COMPANY, INC.]",
      "spl_version": "2",
      "published_date": "2025-12-31"
    }
  },
  "productid": "85642-205_4604a39a-68bf-7dd9-e063-6394a90a5515",
  "productndc": "85642-205",
  "dosage_form": "CREAM",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "ZINC OXIDE",
  "proprietary_name": "Non Tinted Moisturizing Mineral Sunscreen",
  "active_ingred_unit": "mg/g",
  "application_number": "M020",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "Zinc Oxide",
  "start_marketing_date": "20220607",
  "active_numerator_strength": "200"
}

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