Adult Glycerin Laxative

Manufacturer: McKesson
Effective date: 2010-02-22
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 22:23:38

Label at a glance#

ProductAdult Glycerin Laxative

Active ingredientglycerin

Label structure8 sections

Dosage and administration

Adults and children 6 years of age and older: carefully insert one suppository well into the rectum Do not use more than once per day Generally produces a bowel movement in 15 minutes to 1 hour Children under 6 years of age: ask a doctor.

Storage and handling

Store container tightly closed Store at room temperature: 15°- 30° C (59° - 86° F). Do not exceed 30° C (86° F).

Contacts and useful links#

Websitewww.sunmarkbrand.com

www.sunmarkbrand.com

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

Glycerin, USP 80.7%

PURPOSE

OTC - PURPOSE SECTION

Laxative

USE

INDICATIONS & USAGE SECTION

For relief of occasional constipation

WARNINGS

WARNINGS SECTION

For rectal use only. May cause rectal discomfort or a burning sensation.

Do not use

OTC - DO NOT USE SECTION

more than one per day
for a period of longer than one week unless directed by a doctor
laxative products when abdominal pain, nausea, or vominting are present unless directed by a doctor
if seal under product lid is damaged, missing or broken.

Ask a doctor before use

OTC - ASK DOCTOR SECTION

if you have noticed a sudden change in bowel habits that persist over a period of two weeks
if you are pregnant or nursing a baby

OTC - ASK DOCTOR/PHARMACIST SECTION

OTC - WHEN USING SECTION

Stop use and ask a doctor

OTC - STOP USE SECTION

if you have rectal bleeding or fail to have a bowel movement after using a laxative. This may indicate a serious condition.

WARNINGS SECTION

OTC - PREGNANCY OR BREAST FEEDING SECTION

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away.

DIRECTIONS

DOSAGE & ADMINISTRATION SECTION

Adults and children 6 years of age and older: carefully insert one suppository well into the rectum
Do not use more than once per day
Generally produces a bowel movement in 15 minutes to 1 hour
Children under 6 years of age: ask a doctor.

OTHER INFORMATION

STORAGE AND HANDLING SECTION

Store container tightly closed
Store at room temperature: 15°- 30° C (59° - 86° F). Do not exceed 30° C (86° F).

INACTIVE INGREDIENTS

INACTIVE INGREDIENT SECTION

sodium stearate, purified water

PACKAGE LABEL - 25 count

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

sunmark®

COMPARE TO FLEET® ACTIVE INGREDIENT*
NDC 49348-159-05

Laxative
Suppositories
Glycerin

For fast, gentle relief of
occasional constipation

ADULT

25 SUPPOSITORIES

Another Quality Product
Distributed by McKesson
One Post Street, San
Francisco, CA 94104
Money Back Guarantee
Please visit us at
www.sunmarkbrand.com

USE ONLY IF PRINTED INNER SEAL IS NOT BROKEN OR MISSING

*This product is not manufactured or distributed by C.B. Fleet Co., owner of the registered trademark Fleet®.

label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
1251049	glycerin 80.7 % Adult Rectal Suppository	PSN	1
1251049	glycerin 1610 MG Rectal Suppository	SCD	1
1251049	glycerin 1.614 GM Rectal Suppository	SY	1
1251049	glycerin 80.7 % Adult Rectal Suppository	SY	1

DailyMed Pharmacologic Classes#

Class, Version, Type table
Class	Version	Type	Effective
GLYCERIN Pharmacologic Class Indexing	2	Indexing - Pharmacologic Class	20180813

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
49348-159-05	2019-10-21	C162847	48780-1	956f9ecf-ce8e-621f-e053-dbdaa90a74ad	DRUG FACTS
49348-159-09	2019-10-21	C162847	48780-1	956f9ecf-ce8e-621f-e053-dbdaa90a74ad	DRUG FACTS

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
49348-159-05	Adult Glycerin Laxative	25 in 1 JAR	SUPPOSITORY	25		1
49348-159-09	Adult Glycerin Laxative	50 in 1 JAR	SUPPOSITORY	50		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
49348-159	ADULT GLYCERIN LAXATIVE (GLYCERIN) SUPPOSITORY [MCKESSON]	1	Legacy NDC, 2 package rows	20100223_99ea8898-b1d4-4d98-afd2-81ad430c5792.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
49348-159-05	EA - Each	49348-159	c2e00251-5b1b-47df-9f21-a64c32bc0f1f	1	2012-07-24
49348-159-09	EA - Each	49348-159	49d31b4e-3ea8-4a4e-a896-b1977d2c580b	1	2012-07-24

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	SPL version
glycerin	ACTIVE INGREDIENT	PDC6A3C0OX	1
glycerin	ACTIVE MOIETY	PDC6A3C0OX	1
sodium stearate	INACTIVE INGREDIENT	QU7E2XA9TG	1
water	INACTIVE INGREDIENT	059QF0KO0R	1

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 4 matching rows.

Adult Glycerin Laxative
Glycerin
sodium stearate
water

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
49348-159	49348-159-05, 49348-159-09

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
glycerin	PDC6A3C0OX	ACTIB
sodium stearate	QU7E2XA9TG	IACT
water	059QF0KO0R	IACT

Source Document#

Source XML

Inactive ingredient matches#

Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.

Inactive ingredient links page 1 of 1 · 3 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredient	IID ingredient	UNII	Dosage form / route	Potency	Maximum daily exposure	Match
sodium stearate	SODIUM STEARATE	QU7E2XA9TG	TABLET, DELAYED RELEASE / ORAL		10 mg	Exact identifier — unii candidate 3 equally ranked IID candidates
sodium stearate	SODIUM STEARATE	QU7E2XA9TG	TABLET / ORAL	9.48 mg		Exact identifier — unii candidate 3 equally ranked IID candidates
sodium stearate	SODIUM STEARATE	QU7E2XA9TG	TABLET, ORALLY DISINTEGRATING / ORAL	0.85 mg		Exact identifier — unii candidate 3 equally ranked IID candidates

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
d4b0c77c-9a3d-4bae-b4f9-bf6defbdc796			99ea8898-b1d4-4d98-afd2-81ad430c5792	2010-02-22	Warnings	Exact identifier spl id: d4b0c77c-9a3d-4bae-b4f9-bf6defbdc796 spl set id: 99ea8898-b1d4-4d98-afd2-81ad430c5792

Reported adverse events (FAERS/openFDA)#

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