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United States · US · US:85819-441_524384e9-b3f9-4c13-e063-6394a90a8973

WHITENING SUNSCREENANTI WRINKLE

UNIISPL

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

Identification

ManufacturerShantou Oushiya Biotechnology Co.,Ltd
CountryUS (United States)
ATC code
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 1

  • ndc11
    8581944102
    5 APPLICATOR in 1 BOX (85819-441-02) / 1 CREAM in 1 APPLICATOR

Annotations

UNII (FDA Substance ID)
15FIX9V2JP
TITANIUM DIOXIDE
RxCUI 38323
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
  "unii": {
    "unii": "15FIX9V2JP",
    "rxcui": "38323",
    "inchikey": "SOQBVABWOPYFQZ-UHFFFAOYSA-N",
    "display_name": "TITANIUM DIOXIDE",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "TOPICAL",
  "spl_meta": {
    "524384e9-b3f8-4c13-e063-6394a90a8973": {
      "match": "brand_token",
      "title": "WHITENING SUNSCREENANTI WRINKLE CREAM [SHANTOU OUSHIYA BIOTECHNOLOGY CO.,LTD]",
      "spl_version": "1",
      "published_date": "2026-05-22"
    }
  },
  "productid": "85819-441_524384e9-b3f9-4c13-e063-6394a90a8973",
  "productndc": "85819-441",
  "dosage_form": "CREAM",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "TITANIUM DIOXIDE; WATER",
  "proprietary_name": "WHITENING SUNSCREENANTI WRINKLE",
  "active_ingred_unit": "g/1; g/1",
  "application_number": null,
  "marketing_category": "UNAPPROVED HOMEOPATHIC",
  "nonproprietary_name": "WHITENING SUNSCREENANTI WRINKLE",
  "start_marketing_date": "20260521",
  "active_numerator_strength": "8; 52.49"
}

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