Fleet

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
Fleet
Generic name
SODIUM PHOSPHATE, DIBASIC AND SODIUM PHOSPHATE, MONOBASIC
Manufacturer
C.B. Fleet Company, Inc.
Product type
HUMAN OTC DRUG
SPL set ID
f50ba829-16c3-40a7-9822-8d6d00353b33
SPL ID
21c3f93d-2cbb-4ee9-909c-0d99b977a65d
Version
1
Effective date
2024-02-29
Source export date
2026-09-28
Source partition
13
Source file
https://download.open.fda.gov/drug/label/drug-label-0013-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/e78bf8aa9f90ab13e640d254dfbd4fe5bfeca4995ec5f9d51bce3356e249cab7/drug-label-0013-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 06:35:37
Harmonized routes table
Harmonized routes
RECTAL

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 For rectal use only. Using more than one enema in 24 hours can be harmful. Do not use • for more than 3 days • if you have kidney disease • if you have heart problems • if you are dehydrated • when abdominal pain, nausea, or vomiting are present unless directed by a doctor Ask a doctor before using this product if you • are 55 years of age or older • are on a sodium-restricted diet • have a sudden change in bowel habits lasting more than 2 weeks • already used a laxative for more than 1 week Stop use and ask a doctor if you have • rectal bleeding • no bowel movement or no liquid comes out of the rectum after 30 minutes • symptoms of dehydration [feeling thirsty, dizziness, vomiting, urinating less often than normal] These symptoms may indicate a serious condition. If pregnant or breast-feeding , ask a health professional before use. Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) right away.

Reported adverse events (FAERS/openFDA)#

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