GLYCERIN - glycerin suppository 
Chain Drug Consortium LLC

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Premier Value Glycerin Supp

Active ingredient (in each suppository)

Glycerin 2 g

Purpose

Hyperosmotic laxative

Uses

Warnings

For rectal use only

May cause rectal discomfort of 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 for more 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 dosage

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

children 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

Qestions or comments?

1-800-492-5988

Glycerin Suppositories, 50 count

PremVal720.jpg

The product package shown above represents a sample of that currently in use. Additional packaging may also be available.

Glycerin Suppositories, 50 count

Distributed by

Pharmacy Value Alliance, LLC

407 East Lancaster Avenue

Wayne, PA 19087

Premier Value Adult

GLYCERIN  
glycerin suppository
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:68016-015
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:68016-015-81100 in 1 JAR; Type 0: Not a Combination Product03/15/2012
2NDC:68016-015-8050 in 1 JAR; Type 0: Not a Combination Product03/15/2012
3NDC:68016-015-7925 in 1 JAR; Type 0: Not a Combination Product03/15/2012
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM00703/15/2012
Labeler - Chain Drug Consortium LLC (101668460)
Registrant - DSC Laboratories, Inc. (097807374)
Establishment
NameAddressID/FEIBusiness Operations
DSC Laboratories, Inc.097807374manufacture(68016-015)

Revised: 12/2023
Document Id: 0c000c2f-9bdc-c28c-e063-6394a90a455e
Set id: 4694f05b-d927-4e15-9630-a0a1cddb3cbb
Version: 10
Effective Time: 20231208
 
Chain Drug Consortium LLC