GLYCERIN- glycerin suppository 
H E B

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

----------

H E B Adult Glycerin Suppositories

Active ingredient (in each suppository)

Glycerin 2g

Purpose

Laxative

Uses

Warnings

For rectal use only

May cause rectal discomfort or a burning sensation.

Ask a doctor before using any laxative if you have

  • 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

  • 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.

Directions - single daily dose

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

Inactive ingredients

purified water, sodium hydroxide, stearic acid

Questions or comments?

1-800-492-5988

Label

HEB 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

GLYCERIN 
glycerin suppository
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:37808-398
Route of AdministrationRECTAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
GLYCERIN (UNII: PDC6A3C0OX) (GLYCERIN - UNII:PDC6A3C0OX) GLYCERIN2 g
Inactive Ingredients
Ingredient NameStrength
SODIUM HYDROXIDE (UNII: 55X04QC32I)  
STEARIC ACID (UNII: 4ELV7Z65AP)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:37808-398-5050 in 1 JAR; Type 0: Not a Combination Product09/23/2016
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart33409/23/2016
Labeler - H E B (007924756)
Registrant - DSC Laboratories Inc. (097807374)
Establishment
NameAddressID/FEIBusiness Operations
DSC Laboratories Inc.097807374manufacture(37808-398)

Revised: 11/2021
Document Id: cfe43312-3d18-e7fc-e053-2995a90a771f
Set id: 3d03ce42-e671-6d76-e054-00144ff8d46c
Version: 6
Effective Time: 20211103
 
H E B