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United States · US · US:10028-030_36d7d5ec-05de-9e59-e063-6394a90a2654

Ultra UV Protective Daily Moisturising SPF 30 Mineral Sunscreen

UNIISPL

Last synced from FDA National Drug Code directory (United States) on

Identification

ManufacturerUltraceuticals Pty Ltd
CountryUS (United States)
ATC code
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 1

  • ndc11
    1002803002
    1 CARTON in 1 CARTON (10028-030-02) / 75 mL in 1 CARTON (10028-030-01)

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": "10028-030_36d7d5ec-05de-9e59-e063-6394a90a2654",
  "productndc": "10028-030",
  "dosage_form": "CREAM",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "ZINC OXIDE",
  "proprietary_name": "Ultra UV Protective Daily Moisturising SPF 30 Mineral Sunscreen",
  "active_ingred_unit": "g/100mL",
  "application_number": "M020",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "Zinc Oxide",
  "start_marketing_date": "20250605",
  "active_numerator_strength": "14"
}

Access this data programmatically

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