🇺🇸
United States · US · US:68788-7674_a3516560-2440-4bb0-bf1d-3970a07b598c
Stimulant Laxative Plus Stool Softener
UNIISPLATC A06AA
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerPreferred Pharmaceuticals, Inc.
CountryUS (United States)
ATC codeA06AA
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 2
- ndc116878876741100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68788-7674-1)
- ndc11687887674660 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68788-7674-6)
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": {
"0901d005-da72-4eee-a44d-e3a59f1d5aba": {
"match": "brand_token",
"title": "STIMULANT LAXATIVE (SENNOSIDES) TABLET, SUGAR COATED [CVS WOONSOCKET PRESCRIPTION CENTER, INCORPORATED]",
"spl_version": "3",
"published_date": "2026-05-13"
}
},
"productid": "68788-7674_a3516560-2440-4bb0-bf1d-3970a07b598c",
"productndc": "68788-7674",
"dosage_form": "TABLET, FILM COATED",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "DOCUSATE SODIUM; SENNOSIDES",
"proprietary_name": "Stimulant Laxative Plus Stool Softener",
"active_ingred_unit": "mg/1; mg/1",
"application_number": "part334",
"marketing_category": "OTC MONOGRAPH DRUG",
"nonproprietary_name": "Docusate Sodium 50 mg and Sennosides 8.6 mg",
"start_marketing_date": "20200228",
"active_numerator_strength": "50; 8.6"
}Related drugs
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