OUHOE Ultra Anti-Acne Control Gel

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
8516300601
20 mg in 1 BOX (85163-006-01)

Annotations

UNII (FDA Substance ID)

4370DF050B

CERAMIDE NP

RxCUI 1362741

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "4370DF050B",
    "rxcui": "1362741",
    "inchikey": null,
    "display_name": "CERAMIDE NP",
    "substance_type": "mixture",
    "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": "85163-006_448df74a-3d37-8b21-e063-6294a90af122",
  "productndc": "85163-006",
  "dosage_form": "GEL",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "CERAMIDE NP",
  "proprietary_name": "OUHOE Ultra Anti-Acne Control Gel",
  "active_ingred_unit": "mg/20mg",
  "application_number": "M016",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "GLYCERIN",
  "start_marketing_date": "20250808",
  "active_numerator_strength": ".004"
}

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