GLYCERIN- glycerin suppository 
DSC Laboratories Inc.

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DSC Labs Adult Glycerin Suppositories

Active ingredient (in each suppository)

Glycerin 2.1g

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

DSCLabs_50ctThe 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

GLYCERIN 
glycerin suppository
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:52316-725
Route of AdministrationRECTAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
GLYCERIN (UNII: PDC6A3C0OX) (GLYCERIN - UNII:PDC6A3C0OX) GLYCERIN2.1 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:52316-725-5050 in 1 JAR; Type 0: Not a Combination Product04/17/2020
2NDC:52316-725-2525 in 1 JAR; Type 0: Not a Combination Product06/22/202012/11/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM00704/17/2020
Labeler - DSC Laboratories Inc. (097807374)
Registrant - DSC Laboratories Inc. (097807374)
Establishment
NameAddressID/FEIBusiness Operations
DSC Laboratories Inc.097807374manufacture(52316-725)

Revised: 12/2023
Document Id: 0c00a453-546f-acfb-e063-6294a90a9dd3
Set id: a381838b-d1ae-11c5-e053-2a95a90a7bcb
Version: 6
Effective Time: 20231208
 
DSC Laboratories Inc.