Pedia-Lax

openFDA label record#

This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.

Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)

Brand name: Pedia-Lax
Generic name: DOCUSATE SODIUM
Manufacturer: C.B. Fleet Company, Inc.
Product type: HUMAN OTC DRUG
SPL set ID: 0e908bea-ebab-44e7-919c-90002e6f5d42
SPL ID: 6c2dec84-5645-49f0-a3c2-882f4e28d67e
Version: 1
Effective date: 2024-10-01
Source export date: 2026-11-06
Source partition: 10
Source file: https://download.open.fda.gov/drug/label/drug-label-0010-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-11-06/b0d9ca61dc485ebaf55e14a76d7d677668e40ef1e1978cdbcc4d73d58eba0b99/drug-label-0010-of-0014.json.zip
Source manifest SHA-256: 4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
Import run: 20261108T063105Z
Imported at: 2026-11-08 07:47:29

Harmonized routes table
Harmonized routes
ORAL

Harmonized identifier links#

Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.

Harmonized identifiers page 1 of 1 · 12 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M007	openfda.application_number
brand name		Pedia-Lax	openfda.brand_name
generic name		DOCUSATE SODIUM	openfda.generic_name
manufacturer name		C.B. Fleet Company, Inc.	openfda.manufacturer_name
ndc	package	0132-0113-24	openfda.package_ndc
ndc	product	0132-0113	openfda.product_ndc
ndc11	package	00132011324	derived:openfda.package_ndc
rxcui		1088245	openfda.rxcui
rxcui		1088249	openfda.rxcui
spl id		6c2dec84-5645-49f0-a3c2-882f4e28d67e	id
spl set id		0e908bea-ebab-44e7-919c-90002e6f5d42	set_id
unii		F05Q2T2JA0	openfda.unii

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 1 of 1 · 1 matching rows.

warnings

Warnings Drug Interaction Precaution: Do not give this product to your child if your child is presently taking mineral oil, unless directed by a doctor. Ask a doctor before using any laxative if your child has a sudden change in bowel habits lasting more than 2 weeks already used a laxative for more than 1 week If constipation continues after 1 week of use, contact your child's doctor Stop using this product and consult a doctor if your child has rectal bleeding no bowel movement within 72 hours of using this product These symptoms may be signs of a serious condition.

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.