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United States · US · US:69517-131_083396b6-6a49-ffc7-e063-6294a90ad8e2
SENNA-S
UNIISPLATC A06AA
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerHealthLife of USA LLC
CountryUS (United States)
ATC codeA06AA
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 4
- ndc1169517131022 POUCH in 1 POUCH (69517-131-02) / 2 TABLET, COATED in 1 POUCH
- ndc1169517131101000 BOTTLE in 1 BOTTLE (69517-131-10) / 500 BOTTLE in 1 BOTTLE (69517-131-05) / 24 CARTON in 1 BOTTLE (69517-131-24) / 1 TABLET, COATED in 1 CARTON
- ndc11695171312525 POUCH in 1 BOX (69517-131-25) / 2 TABLET, COATED in 1 POUCH
- ndc11695171315050 POUCH in 1 BOX (69517-131-50) / 2 TABLET, COATED in 1 POUCH
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": {
"d148be81-79b4-41f7-b8d8-a0e85b661592": {
"match": "brand_token",
"title": "SENNA-S (DOCUSATE SODIUM AND SENNOSIDES) TABLET [ADVANCED RX LLC]",
"spl_version": "2",
"published_date": "2026-02-19"
}
},
"productid": "69517-131_083396b6-6a49-ffc7-e063-6294a90ad8e2",
"productndc": "69517-131",
"dosage_form": "TABLET, COATED",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "DOCUSATE SODIUM; SENNOSIDES",
"proprietary_name": "SENNA-S",
"active_ingred_unit": "mg/1; mg/1",
"application_number": "505G(a)(3)",
"marketing_category": "OTC MONOGRAPH DRUG",
"nonproprietary_name": "Senna and Docusate Sodium Tablets, 8.6 mg and 50 mg",
"start_marketing_date": "20160307",
"active_numerator_strength": "50; 8.6"
}Related drugs
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