Ultra Zinc Physical Defense

UNIISPL

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

Identification

ManufacturerATLANTA DERMOTOLOGY VEIN & RESEARCH CENTER

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
8549920515
1.5 g in 1 PACKET (85499-205-15)

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": {
    "52d4b1c1-7431-4f8c-e063-6294a90ad482": {
      "match": "brand_token",
      "title": "ULTRA VIOLETTE VELVET SCREEN BLURRING MINERAL SKINSCREEN BROAD SPECTRUM SPF 40 (ZINC OXIDE) CREAM [GRACE AND FIRE USA INC.]",
      "spl_version": "1",
      "published_date": "2026-05-29"
    }
  },
  "productid": "85499-205_4600a3ec-a70a-9b43-e063-6294a90abfab",
  "productndc": "85499-205",
  "dosage_form": "CREAM",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "ZINC OXIDE",
  "proprietary_name": "Ultra Zinc Physical Defense",
  "active_ingred_unit": "mg/g",
  "application_number": "M020",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "Zinc Oxide",
  "start_marketing_date": "20220406",
  "active_numerator_strength": "200"
}

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