Glycerin by DSC Laboratories Inc. GLYCERIN suppository

Glycerin by

Drug Labeling and Warnings

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

Drug Details [pdf]

Active ingredient (in each suppository)

Glycerin 2.1g

Purpose

Laxative

Uses

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

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 dosage

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

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

Inactive ingredients

purified water, sodium hydroxide, stearic acid

Questions or comments?

1-800-492-5988

Label

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

Adult Glycerin Suppositories, 50 count

Manufactured by

DSC Laboratories Inc.

1979 Latimer Dr.

Muskegon, MI 49442 USA

DSCLabs_50ct

INGREDIENTS AND APPEARANCE

GLYCERIN 
glycerin suppository

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 52316-725
Route of Administration	RECTAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
GLYCERIN (UNII: PDC6A3C0OX) (GLYCERIN - UNII:PDC6A3C0OX)	GLYCERIN	2.1 g

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

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 52316-725-50	50 in 1 JAR; Type 0: Not a Combination Product	04/17/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part334	04/17/2020

Labeler - DSC Laboratories Inc. (097807374)

Registrant - DSC Laboratories Inc. (097807374)

Establishment
Name	Address	ID/FEI	Business Operations
DSC Laboratories Inc.		097807374	manufacture(52316-725)