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United States · US · US:84324-030_733d1bb6-dc55-4ca4-96f8-6c418b0b5ea8
Senna-S Softgel
UNIISPLATC A06AA
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerNUVICARE LLC
CountryUS (United States)
ATC codeA06AA
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc11843240300160 CAPSULE, LIQUID FILLED in 1 BOTTLE (84324-030-01)
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": "84324-030_733d1bb6-dc55-4ca4-96f8-6c418b0b5ea8",
"productndc": "84324-030",
"dosage_form": "CAPSULE, LIQUID FILLED",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "DOCUSATE SODIUM; SENNOSIDES",
"proprietary_name": "Senna-S Softgel",
"active_ingred_unit": "mg/1; mg/1",
"application_number": "505G(a)(3)",
"marketing_category": "OTC MONOGRAPH DRUG",
"nonproprietary_name": "Sennosides 8.6 mg and Docusate Sodium 50 mg",
"start_marketing_date": "20250624",
"active_numerator_strength": "50; 8.6"
}Related drugs
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