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United States · US · US:70000-0520_1e126b6e-0087-44e7-84ed-c8046f497c0c
Senna Plus
UNIISPLATC A06AA
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerCARDINAL HEALTH, 110 DBA LEADER
CountryUS (United States)
ATC codeA06AA
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc11700000520130 BOTTLE, PLASTIC in 1 CARTON (70000-0520-1) / 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
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": {
"491255c6-465f-a78a-e063-6394a90aa408": {
"match": "brand_token",
"title": "SENNA SYRUP (SENNOSIDES 8.8MG/5ML) SOLUTION [ALDAMA PHARMACEUTICALS, INC]",
"spl_version": "2",
"published_date": "2026-06-02"
}
},
"productid": "70000-0520_1e126b6e-0087-44e7-84ed-c8046f497c0c",
"productndc": "70000-0520",
"dosage_form": "TABLET, FILM COATED",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "DOCUSATE SODIUM; SENNOSIDES",
"proprietary_name": "Senna Plus",
"active_ingred_unit": "mg/1; mg/1",
"application_number": "M007",
"marketing_category": "OTC MONOGRAPH DRUG",
"nonproprietary_name": "Docusate Sodium 50 mg and Sennosides 8.6 mg",
"start_marketing_date": "20191023",
"active_numerator_strength": "50; 8.6"
}Related drugs
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