RENEWALUXE SPF 50 Sunscreen

UNIISPL

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

Identification

ManufacturerGuangzhou Fantesy Biotechnology Co.,Ltd

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
8344700501
50 mL in 1 BOX (83447-005-01)

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": "CUTANEOUS",
  "spl_meta": {
    "1bc29960-5e73-e8ab-e063-6294a90a3f80": {
      "match": "brand_token",
      "title": "RENEWALUXE SPF 50 SUNSCREEN CREAM [GUANGZHOU FANTESY BIOTECHNOLOGY CO.,LTD]",
      "spl_version": "4",
      "published_date": "2026-01-07"
    }
  },
  "productid": "83447-005_47b31ef5-e027-ed4b-e063-6294a90a2d30",
  "productndc": "83447-005",
  "dosage_form": "CREAM",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "ZINC OXIDE",
  "proprietary_name": "RENEWALUXE SPF 50 Sunscreen",
  "active_ingred_unit": "g/100mL",
  "application_number": "M020",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "RENEWALUXE SPF 50 Sunscreen",
  "start_marketing_date": "20240626",
  "active_numerator_strength": "21.8"
}

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