GLYCERIN- glycerin suppository

Glycerin by

Drug Labeling and Warnings

Glycerin by is a Otc medication manufactured, distributed, or labeled by Chain Drug Consortium LLC, DSC Laboratories, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient (in each suppository)

Glycerin 1 g

Purpose

Hyperosmotic laxative

Uses

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

Warnings

For rectal use only

May cause rectal discomfort of burning sensation

Ask a Doctor before using laxative if child has

• abdominal pain, nausea or vomiting
• a sudden change in bowel habits lasting more than two 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

• children 2 to under 6 years: 1 suppository or as directed by a doctor
• children under 2 years: ask a doctor

Insert suppository well up intorectum.

Suppository need not melt completely to produce laxative action.

Other information

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

Inactive ingredients

purified water, sodium hydroxide, stearic acid

Pediatric Glycerin Suppositories, 25 count

PremVal722.jpg

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

PediatricGlycerin Suppositories, 25 count

Distributed by Pharmacy Value Alliance, LLC

407 East Lancaster Avenue

Wayne, PA 19087

INGREDIENTS AND APPEARANCE

GLYCERIN  
glycerin suppository

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 68016-161
Route of Administration	RECTAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
GLYCERIN (UNII: PDC6A3C0OX) (GLYCERIN - UNII:PDC6A3C0OX)	GLYCERIN	1 g

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
STEARIC ACID (UNII: 4ELV7Z65AP)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 68016-161-00	25 in 1 JAR; Type 0: Not a Combination Product	03/21/2012

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part334	03/21/2012

Labeler - Chain Drug Consortium LLC (101668460)

Registrant - DSC Laboratories, Inc. (097807374)

Establishment
Name	Address	ID/FEI	Business Operations
DSC Laboratories, Inc.		097807374	manufacture(68016-161)