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: GLYCERIN
Manufacturer: C.B. Fleet Company, Inc.
Product type: HUMAN OTC DRUG
SPL set ID: 381f4179-0c3b-41f8-927c-c88534ebe06d
SPL ID: f2cecd21-3558-41f0-9fbb-d6cf532bd0ab
Version: 8
Effective date: 2024-05-06
Source export date: 2026-10-27
Source partition: 7
Source file: https://download.open.fda.gov/drug/label/drug-label-0007-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-27/be847f9aea8d80a2cb7e9771acd1143be084664192ecf8f5be8ac1024116f4f0/drug-label-0007-of-0014.json.zip
Source manifest SHA-256: 6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
Import run: 20261027T193451Z
Imported at: 2026-10-27 20:17:07

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 · 13 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		GLYCERIN	openfda.generic_name
manufacturer name		C.B. Fleet Company, Inc.	openfda.manufacturer_name
ndc	package	0132-0185-01	openfda.package_ndc
ndc	package	0132-0185-82	openfda.package_ndc
ndc	product	0132-0185	openfda.product_ndc
ndc11	package	00132018582	derived:openfda.package_ndc
ndc11	package	00132018501	derived:openfda.package_ndc
rxcui		596936	openfda.rxcui
spl id		f2cecd21-3558-41f0-9fbb-d6cf532bd0ab	id
spl set id		381f4179-0c3b-41f8-927c-c88534ebe06d	set_id
unii		PDC6A3C0OX	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 May cause rectal discomfort or a burning sensation. 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 any laxative if you have a sudden change in bowel habits lasting more than 2 weeks already used a laxative for more than 1 week Stop using this product and consult a doctor if you have rectal bleeding no bowel movement within 1 hour of using this product These symptoms may indicate a serious condition. 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.