Glycerin description, usages, side effects, indications, overdosage, supplying and lots more!

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Glycerin

G&W Laboratories, Inc.
G&W Laboratories, Inc.

Adult Glycerin


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

ACTIVE INGREDIENT (in each suppository)

Glycerin, USP 2.1 grams

PURPOSE

Laxative

USE

• relieves occasional constipation (irregularity)
• generally produces bowel movement in 1/4 to 1 hour

WARNINGS

For rectal use only
Do not use
laxative products for longer than 1 week unless directed by a doctor

Ask a doctor before use if you have
• stomach pain
• nausea
• vomiting
• noticed a sudden change in bowel habits that lasts over 2 weeks

When using this product
you may have rectal discomfort or a burning sensation

Stop use and ask a doctor
if you have rectal bleeding or fail to have a bowel movement after use of a laxative. These could be signs of a serious condition.

IF PREGNANT OR BREAST FEEDING

 ask a health professional before use.

KEEP OUT OF REACH OF CHILDREN

If swallowed, get medical help or contact a Poison Control Center right away.

DIRECTIONS

adults and children 6 years and over 1 suppository per day or as directed by a doctor
children 2 to under 6 years use pediatric glycerin suppositories
children under 2 years ask a doctor

• insert 1 suppository well up into rectum and retain for 15 minutes
• it need not melt to produce laxative action

OTHER INFORMATION

• keep tightly closed
• avoid excessive heat

INACTIVE INGREDIENT

purified water, sodium hydroxide, stearic acid

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC 0713-0101-02
Glycerin Suppositories
Laxative
100 Adult Size

Glycerin

Glycerin SUPPOSITORY

Product Information

Product Type Human otc drug label Item Code (Source) NDC:0713-0101
Route of Administration RECTAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
GLYCERIN 2.1 g

Inactive Ingredients

Ingredient Name Strength
water
SODIUM HYDROXIDE
STEARIC ACID

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:0713-0101-02 100 in 1 JAR
2 NDC:0713-0101-13 12 in 1 JAR
3 NDC:0713-0101-25 25 in 1 CARTON
4 NDC:0713-0101-26 25 in 1 JAR
5 NDC:0713-0101-51 51 in 1 JAR
6 NDC:0713-0101-09 10 in 1 CARTON

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part334 1987-06-08


PLEASE, BE CAREFUL!
Be sure to consult your doctor before taking any medication!
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