Ultimate Mineral Protection

UNIISPL

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

Identification

ManufacturerMARK SCHWARTZ CLINICAL SKINCARE, INC.

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
8571520504
113 g in 1 BOTTLE, PUMP (85715-205-04)

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": {
    "35bc5ff5-8eb8-54cf-e063-6394a90ae3c2": {
      "match": "brand_token",
      "title": "ULTIMATE PHYSICAL SUNSCREEN (ZINC OXIDE) CREAM [HALEM DERMATOLOGY PLLC]",
      "spl_version": "2",
      "published_date": "2025-12-12"
    }
  },
  "productid": "85715-205_458b49d0-0460-0e6e-e063-6294a90a7828",
  "productndc": "85715-205",
  "dosage_form": "CREAM",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "ZINC OXIDE",
  "proprietary_name": "Ultimate Mineral Protection",
  "active_ingred_unit": "mg/g",
  "application_number": "M020",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "Zinc Oxide",
  "start_marketing_date": "20211206",
  "active_numerator_strength": "200"
}

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