WOODSLEEP Tallow Sunscreen

SPL

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

Identification

ManufacturerShantou Woodsleep Biotechnology Co., Ltd.

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
8505300201
57 mg in 1 BOX (85053-002-01)

Annotations

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "route": "TOPICAL",
  "spl_meta": {
    "45cfc7ed-34a6-1f45-e063-6394a90a902b": {
      "match": "brand_token",
      "title": "WOODSLEEP SUNSCREEN BALM (TITANIUM DIOXIDE) CREAM [SHANTOU WOODSLEEP BIOTECHNOLOGY CO., LTD.]",
      "spl_version": "1",
      "published_date": "2025-12-15"
    }
  },
  "productid": "85053-002_448bdbfa-2de6-fce8-e063-6394a90a2cf7",
  "productndc": "85053-002",
  "dosage_form": "CREAM",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "TALLOW",
  "proprietary_name": "WOODSLEEP Tallow Sunscreen",
  "active_ingred_unit": "mg/57mg",
  "application_number": "M020",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "TITANIUM DIOXIDE",
  "start_marketing_date": "20250418",
  "active_numerator_strength": ".0114"
}

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