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: 2528cb5e-437e-41f0-9c34-e9ce57404d8b
SPL ID: 749b7e47-7344-44ec-a526-0c7dc18680f2
Version: 14
Effective date: 2023-10-26
Source export date: 2026-09-28
Source partition: 4
Source file: https://download.open.fda.gov/drug/label/drug-label-0004-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/c7ca0b7091cdaeab3f27713a6eef00adcf8fe722383633ddce61531b4c840544/drug-label-0004-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:23:54

Harmonized routes table
Harmonized routes
RECTAL

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 · 11 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M007	openfda.application_number
brand name		FLEET	openfda.brand_name
generic name		MINERAL OIL	openfda.generic_name
manufacturer name		C.B. Fleet Company, Inc.	openfda.manufacturer_name
ndc	package	0132-0301-40	openfda.package_ndc
ndc	product	0132-0301	openfda.product_ndc
ndc11	package	00132030140	derived:openfda.package_ndc
rxcui		205121	openfda.rxcui
spl id		749b7e47-7344-44ec-a526-0c7dc18680f2	id
spl set id		2528cb5e-437e-41f0-9c34-e9ce57404d8b	set_id
unii		T5L8T28FGP	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 For rectal use only . Do not use when abdominal pain, nausea, or vomiting are present unless directed by a doctor. Ask a doctor before using this product if you 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 within 15 minutes of using this product 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 right away.

Reported adverse events (FAERS/openFDA)#

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