Gene 16 Whitening Factor

UNIISPL

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

Identification

ManufacturerShanghai Liangliang Bio Technology Co., Ltd

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
6976400110
1 POUCH in 1 PACKAGE (69764-001-10) / 7 mg in 1 POUCH

Annotations

UNII (FDA Substance ID)

344S277G0Z

ALLANTOIN

RxCUI 508

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "344S277G0Z",
    "rxcui": "508",
    "inchikey": "POJWUDADGALRAB-UHFFFAOYSA-N",
    "display_name": "ALLANTOIN",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "TOPICAL",
  "spl_meta": {
    "b0a99964-d906-4c1d-8256-8c18dd9f88a6": {
      "match": "brand_token",
      "title": "GENE 16 WHITENING FACTOR (ALLANTOIN) TABLET, SOLUBLE [SHANGHAI LIANGLIANG BIO TECHNOLOGY CO., LTD]",
      "spl_version": "33037",
      "published_date": "2026-01-26"
    }
  },
  "productid": "69764-001_292b677d-cbe2-4962-9406-123e272e54ea",
  "productndc": "69764-001",
  "dosage_form": "TABLET, SOLUBLE",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "ALLANTOIN",
  "proprietary_name": "Gene 16 Whitening Factor",
  "active_ingred_unit": "mg/100mg",
  "application_number": "M016",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "Allantoin",
  "start_marketing_date": "20140925",
  "active_numerator_strength": ".5"
}

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