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
MINERAL OIL
Manufacturer
C.B. Fleet Company, Inc.
Product type
HUMAN OTC DRUG
SPL set ID
e0b7acab-add4-4daf-b1df-bb7cf5ca8e19
SPL ID
be2908e5-b58b-4d3c-b284-ee31cf2f088d
Version
1
Effective date
2024-04-01
Source export date
2026-09-28
Source partition
9
Source file
https://download.open.fda.gov/drug/label/drug-label-0009-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/6784607726c827491ceaeab30d843632e0660ee8008c535197be5ed9e1e52201/drug-label-0009-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 06:03:47
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 Do not use ▪ for children under 6 years of age, pregnant women, bedridden patients or persons with difficulty swallowing Ask a doctor before using this product if you have ▪ abdominal pain, nausea or vomiting ▪ a sudden change in bowel habits that persists over a period of 2 weeks Ask a doctor or pharmacist before use if you are presently taking a stool softener laxative. When using this product do not take with meals. Stop use and ask a doctor if ▪ you notice rectal bleeding or fail to have a bowel movement after use of a laxative. This may indicate a serious condition. Discontinue use and consult a doctor. ▪ you need to use the product more than one week If breast-feeding, ask a health professional before use. Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.

Reported adverse events (FAERS/openFDA)#

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