GLYCERIN- glycerin suppository 
DSC Laboratories Inc.

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Core Values Adult Glycerin Suppositories

Active ingredient (in each suppository)

Glycerin 2g

Purpose

Laxative

Uses

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

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

Distributed by

Liberty Procurement Inc.

650 Liberty Ave.

Union, NJ 07083 USA

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GLYCERIN 
glycerin suppository
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:52316-720
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:52316-720-5150 in 1 JAR; Type 0: Not a Combination Product08/01/2017
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM00708/01/2017
Labeler - DSC Laboratories Inc. (097807374)
Registrant - DSC Laboratories Inc. (097807374)
Establishment
NameAddressID/FEIBusiness Operations
DSC Laboratories Inc.097807374manufacture(52316-720)

Revised: 12/2023
Document Id: 0c00b4f6-ff1f-df94-e063-6394a90a96da
Set id: 5d8e5726-5401-898c-e053-2991aa0aca76
Version: 8
Effective Time: 20231208
 
DSC Laboratories Inc.