GLYCERIN - glycerin suppository 
Chain Drug Marketing Association Inc.

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Quality Choice Pediatric Glycerin Supp

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

Pediatric Glycerin Suppositories, 25 count

QCPediatric25ct

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 C.D.M.A. Inc.

43157 W. Nine Mile

Novi, MI 48376-0995

www.qualitychoice.com

QC Pediatric25ct.jpg

GLYCERIN  
glycerin suppository
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:63868-282
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:63868-282-2525 in 1 JAR; Type 0: Not a Combination Product03/20/2012
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM00703/20/2012
Labeler - Chain Drug Marketing Association Inc. (011920774)
Registrant - DSC Laboratories Inc. (097807374)
Establishment
NameAddressID/FEIBusiness Operations
DSC Laboratories Inc.097807374manufacture(63868-282)

Revised: 12/2023
Document Id: 0c00ce56-67e2-c716-e063-6294a90a52eb
Set id: 5e84a72c-868d-396b-e053-2991aa0a5787
Version: 7
Effective Time: 20231208
 
Chain Drug Marketing Association Inc.