OUHOE Daily Exposure Lightweight Sunscreen

UNIISPL

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

Identification

ManufacturerShantou Ouhoe Technology Co., Ltd.

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
8516301301
60 mg in 1 BOTTLE, PLASTIC (85163-013-01)

Annotations

UNII (FDA Substance ID)

6810070TYD

CENTELLA ASIATICA LEAF

RxCUI 1307961

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "6810070TYD",
    "rxcui": "1307961",
    "inchikey": null,
    "display_name": "CENTELLA ASIATICA LEAF",
    "substance_type": "structurallyDiverse",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "TOPICAL",
  "spl_meta": {
    "46d36f60-2a5d-816e-e063-6294a90a2ddc": {
      "match": "brand_token",
      "title": "OUHOE FACE BODY SUNSCREEN (TITANIUM DIOXIDE) CREAM [SHANTOU OUHOE TECHNOLOGY CO., LTD.]",
      "spl_version": "1",
      "published_date": "2025-12-29"
    }
  },
  "productid": "85163-013_454301b6-21a7-6153-e063-6294a90a1366",
  "productndc": "85163-013",
  "dosage_form": "CREAM",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "CENTELLA ASIATICA LEAF",
  "proprietary_name": "OUHOE Daily Exposure Lightweight Sunscreen",
  "active_ingred_unit": "mg/60mg",
  "application_number": "M020",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "TITANIUM DIOXIDE",
  "start_marketing_date": "20251206",
  "active_numerator_strength": ".012"
}

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