Glycerin

Manufacturer
H E B | DSC Laboratories Inc.
Effective date
2025-10-24
Label type
HUMAN OTC DRUG LABEL
Version
10
Source
full-release
Hydrated at
2026-06-01 01:40:00

Label at a glance#

ProductGlycerin
Active ingredientGLYCERIN
Label structure9 sections

Indications and uses

for relief of occassional constipation this product generally produces bowel movement in 1/4 to 1 hour

Dosage and administration

adult and children 6 years and over - 1 suppository, or as directed by a doctor chidren 2 to under 6 years - use Child Suppositories Insert suppository well up into rectum. Suppository need not melt completely to produce laxative action.

Label contents#

Full prescribing information#

Active ingredient (in each suppository)

OTC - ACTIVE INGREDIENT SECTION

Glycerin 2g

Purpose

OTC - PURPOSE SECTION

Laxative

Uses

INDICATIONS & USAGE SECTION

  • for relief of occassional constipation
  • this product generally produces bowel movement in 1/4 to 1 hour

Warnings

WARNINGS SECTION

For rectal use only

May cause rectal discomfort or a burning sensation.

Ask a doctor before using any laxative if you have

OTC - ASK DOCTOR SECTION

  • abdominal pain, nausea or vomiting
  • a sudden change in bowel habits lasting more than 2 weeks
  • already used a laxative formore than 1 week

Stop use and consult a doctor if you have

OTC - STOP USE SECTION

  • rectal bleeding
  • no bowel movement after 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.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Directions - single daily dose

DOSAGE & ADMINISTRATION SECTION

adult and children 6 years and over - 1 suppository, or as directed by a doctor

chidren 2 to under 6 years - use Child Suppositories

Insert suppository well up into rectum. Suppository need not melt completely to produce laxative action.

Other information

OTHER SAFETY INFORMATION

  • Store container tightly closed.
  • Keep away from excessive heat.

Inactive ingredients

INACTIVE INGREDIENT SECTION

purified water, sodium hydroxide, stearic acid

Questions or comments?

OTC - QUESTIONS SECTION

1-800-492-5988

Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

HEB Adult 50ct Glycerin SuppHEB Adult 50ct Glycerin SuppThe product package shown above represents a sample of that currently in use. Additional packaging may also be available.

Adult Glycerin Suppositories, 50 count

Distributed by H-E-B, San Antonio, TX 78204 1002

HEBAdult50.jpg

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
104155glycerin 2 GM Rectal SuppositoryPSN10
104155glycerin 2000 MG Rectal SuppositorySCD10
104155glycerin 2 GM Rectal SuppositorySY10

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
GLYCERIN Pharmacologic Class Indexing2Indexing - Pharmacologic Class20180813

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
37808-398-50Glycerin50 in 1 JARSUPPOSITORY5010

Products#

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

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

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
37808-39837808-398-50

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
92024-12-12full-release2026-06-01 00:43:08

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
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
GlycerinGLYCERINH E B3d03ce42-e671-6d76-e054-00144ff8d46c2025-10-24WarningsExact identifier
ndc (package): 37808-398-50
ndc (product): 37808-398
ndc11 (package): 37808039850
spl id: 41e9d877-5f13-595d-e063-6394a90a3f50
spl set id: 3d03ce42-e671-6d76-e054-00144ff8d46c

Reported adverse events (FAERS/openFDA)#

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