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United States · US · US:0132-0113_6c2dec84-5645-49f0-a3c2-882f4e28d67e
Pedia-Lax
UNIISPLATC A06AG10
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerC.B. Fleet Company, Inc.
CountryUS (United States)
ATC codeA06AG10
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc110132011324118 mL in 1 CARTON (0132-0113-24)
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": {
"4e15f6ca-a40c-485f-be3f-07c2ed7cb498": {
"match": "brand_token",
"title": "PEDIA-LAX (GLYCERIN) LIQUID [C.B. FLEET COMPANY, INC.]",
"spl_version": "11",
"published_date": "2025-01-20"
}
},
"productid": "0132-0113_6c2dec84-5645-49f0-a3c2-882f4e28d67e",
"productndc": "0132-0113",
"dosage_form": "LIQUID",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "DOCUSATE SODIUM",
"proprietary_name": "Pedia-Lax",
"active_ingred_unit": "mg/15mL",
"application_number": "M007",
"marketing_category": "OTC MONOGRAPH DRUG",
"nonproprietary_name": "Docusate Sodium",
"start_marketing_date": "20230228",
"active_numerator_strength": "50"
}Related drugs
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