Docu Liquid

UNIISPLATC A06AG10

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

Identification

ManufacturerATLANTIC BIOLOGICALS CORP.

CountryUS (United States)

ATC codeA06AG10

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 0

No packs registered.

Annotations

UNII (FDA Substance ID)

F05Q2T2JA0

DOCUSATE SODIUM

RxCUI 71722

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "F05Q2T2JA0",
    "rxcui": "71722",
    "inchikey": "APSBXTVYXVQYAB-UHFFFAOYSA-M",
    "display_name": "DOCUSATE SODIUM",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "f4ed0721-3be9-4108-a6c9-dbbe115249e9": {
      "match": "brand_token",
      "title": "DOCU LIQUID (DOCUSATE SODIUM) LIQUID [ATLANTIC BIOLOGICALS CORP.]",
      "spl_version": "3",
      "published_date": "2025-08-04"
    }
  },
  "productid": "17856-0771_3b3f3045-55db-5ed5-e063-6294a90aab75",
  "productndc": "17856-0771",
  "dosage_form": "LIQUID",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "DOCUSATE SODIUM",
  "proprietary_name": "Docu Liquid",
  "active_ingred_unit": "mg/5mL",
  "application_number": "M",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "Docusate Sodium",
  "start_marketing_date": "19970801",
  "active_numerator_strength": "50"
}

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