GLYCERIN - glycerin suppository 
DSC Laboratories Inc.

----------

Best Choice Pediatric Glycerin Suppositories

Active ingredient (in each suppository)

Glycerin 1.2 g

Purpose

Laxative

Uses

Warnings

For rectal use only

May cause rectal discomfort or a burning sensation

Ask a Doctor before using any laxative if child has

  • 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 child has

  • 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 right away.

Directions

Single daily dosage

childrien 2 to under 6-1 suppository, or as directed by a doctor

children under 2 years-ask a doctor

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

1-800-492-5988

Pediatric Glycerin Suppositories, 25 count

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

PediatricGlycerin Suppositories, 25 count

Distributed by Valu Merchandisers

5000 Kansas Ave.

Kansas City, KS 66106

PedGlycSupp25ct

BestChoicPedSupp

GLYCERIN  
glycerin suppository
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:52316-724
Route of AdministrationRECTAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
GLYCERIN (UNII: PDC6A3C0OX) (GLYCERIN - UNII:PDC6A3C0OX) GLYCERIN1.2 g
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
SODIUM HYDROXIDE (UNII: 55X04QC32I)  
STEARIC ACID (UNII: 4ELV7Z65AP)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:52316-724-2525 in 1 JAR; Type 0: Not a Combination Product08/15/2012
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM00708/15/2012
Labeler - DSC Laboratories Inc. (097807374)
Registrant - DSC Laboratories Inc. (097807374)
Establishment
NameAddressID/FEIBusiness Operations
DSC Laboratories Inc.097807374manufacture(52316-724)

Revised: 12/2023
Document Id: 0c0071e9-7f06-dfdb-e063-6394a90af616
Set id: 5e97c4d2-e41d-5bb6-e053-2a91aa0a3163
Version: 7
Effective Time: 20231208
 
DSC Laboratories Inc.