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
2026-09-28
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/2026-09-28/4bbc9760f647649b787710953d978bd6419e899ba8b90f32c3d972aae43947f8/drug-label-0010-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 06:09:26
Harmonized routes table
Harmonized routes
ORAL

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.