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: 31778652-e60e-4098-8e90-3e4f56b5800c
SPL ID: 4b630f2e-70f2-49ed-8187-30bfe1f7ee92
Version: 5
Effective date: 2026-03-06
Source export date: 2026-11-06
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/2026-11-06/824fe785252d7061429a95ddb6de517ee399ef628d34e8fdcc3591ded286ae33/drug-label-0007-of-0014.json.zip
Source manifest SHA-256: 4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
Import run: 20261108T063105Z
Imported at: 2026-11-08 07:27:17

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 · 17 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	0132-0075-12	openfda.package_ndc
ndc	package	0132-0075-00	openfda.package_ndc
ndc	package	0132-0075-50	openfda.package_ndc
ndc	package	0132-0075-24	openfda.package_ndc
ndc	product	0132-0075	openfda.product_ndc
ndc11	package	00132007524	derived:openfda.package_ndc
ndc11	package	00132007550	derived:openfda.package_ndc
ndc11	package	00132007500	derived:openfda.package_ndc
ndc11	package	00132007512	derived:openfda.package_ndc
rxcui		104155	openfda.rxcui
spl id		4b630f2e-70f2-49ed-8187-30bfe1f7ee92	id
spl set id		31778652-e60e-4098-8e90-3e4f56b5800c	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 For rectal use only. Do not use laxative products 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 When using this product rectal discomfort or burning sensation may occur. 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 (1-800-222-1222) right away.

Reported adverse events (FAERS/openFDA)#

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