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United States · US · US:54257-089_08bf70ec-89e8-36e5-e063-6294a90a6772
Senna S
UNIISPLATC A06AA
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerMagno-Humphries, Inc.
CountryUS (United States)
ATC codeA06AA
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc115425708902100 TABLET in 1 BOTTLE (54257-089-02)
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": "54257-089_08bf70ec-89e8-36e5-e063-6294a90a6772",
"productndc": "54257-089",
"dosage_form": "TABLET",
"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": "M007",
"marketing_category": "OTC MONOGRAPH DRUG",
"nonproprietary_name": "DOCUSATE SODIUM, SENNOSIDES",
"start_marketing_date": "20200124",
"active_numerator_strength": "50; 8.6"
}Related drugs
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