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United States · US · US:21130-883_7645f18f-a849-4fc6-9661-0591c511bae6
Senna S
UNIISPLATC A06AA
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerSafeway, Inc.
CountryUS (United States)
ATC codeA06AA
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc1121130883301 BOTTLE, PLASTIC in 1 BOX (21130-883-30) / 30 TABLET 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": "21130-883_7645f18f-a849-4fc6-9661-0591c511bae6",
"productndc": "21130-883",
"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": "505G(a)(3)",
"marketing_category": "OTC MONOGRAPH DRUG",
"nonproprietary_name": "DOCUSATE SODIUM, SENNOSIDES",
"start_marketing_date": "20191129",
"active_numerator_strength": "50; 8.6"
}Related drugs
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