WOODSLEEP Sunscreen Balm

UNIISPL

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
8505300401
60 mg in 1 BOTTLE, GLASS (85053-004-01)

Annotations

UNII (FDA Substance ID)

2JYC99Q0WZ

ARTEMISIA ARGYI LEAF

RxCUI 1307649

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "2JYC99Q0WZ",
    "rxcui": "1307649",
    "inchikey": null,
    "display_name": "ARTEMISIA ARGYI LEAF",
    "substance_type": "structurallyDiverse",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "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": "85053-004_45cfc7ed-34a7-1f45-e063-6394a90a902b",
  "productndc": "85053-004",
  "dosage_form": "CREAM",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "ARTEMISIA ARGYI LEAF",
  "proprietary_name": "WOODSLEEP Sunscreen Balm",
  "active_ingred_unit": "mg/60mg",
  "application_number": "M020",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "TITANIUM DIOXIDE",
  "start_marketing_date": "20251213",
  "active_numerator_strength": ".012"
}

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