GLYCERIN - glycerin suppository 
LOHXA

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Adult Glycerin Supp.

Active ingredient (in each suppository)

Glycerin 2 g

Purpose

Laxative

Uses

Warnings

For rectal use only

May cause rectal discomfort of 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 for more 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

adults and children 6 years and over - 1 suppository, or as directed by a doctor

children 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

Glycerin Suppositories, 25 count

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

Glycerin Suppositories, 25 count

Repackaged by:

Lohxa

Worcester MA 01608 USA

Adult Glycerin Suppositories

GLYCERIN  
glycerin suppository
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:70166-311(NDC:69842-724)
Route of AdministrationRECTAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
GLYCERIN (UNII: PDC6A3C0OX) (GLYCERIN - UNII:PDC6A3C0OX) GLYCERIN2 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:70166-311-2525 in 1 BOX10/14/2019
11 in 1 POUCH; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart33410/14/2019
Labeler - LOHXA (079872715)

Revised: 10/2019
Document Id: 959c9579-13dd-ad98-e053-2a95a90a0062
Set id: b308e825-de5a-4a21-a094-11b96845fd58
Version: 1
Effective Time: 20191023
 
LOHXA