Label: FLEET- glycerin suppository
- NDC Code(s): 0132-0079-00
- Packager: C.B. Fleet Company, Inc.
- Category: HUMAN OTC DRUG LABEL
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Updated July 2, 2020
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- Active Ingredient
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 for more than 1 week
Stop use and consult a doctor if you have
- rectal bleeding
- no bowel movement within 1 hour of using this product
These symptoms may indicate a serious condition.
Single Daily Dosage (per 24 hours)
adults and children 6 years and over 1 suppository, or as directed by a doctor children 2 to under 6 years use Fleet® Pedia-Lax Suppositories® children under 2 years ask a doctor
Insert suppository well up into rectum. To product laxative action suppository is designed to dissolve only partially, which may not be noticeable.
- Other information
- Inactive ingredients
- PRINCIPAL DISPLAY PANEL
INGREDIENTS AND APPEARANCE
Product Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0132-0079 Route of Administration RECTAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength GLYCERIN (UNII: PDC6A3C0OX) (GLYCERIN - UNII:PDC6A3C0OX) GLYCERIN 2 g Inactive Ingredients Ingredient Name Strength ALOE (UNII: V5VD430YW9) EDETATE DISODIUM (UNII: 7FLD91C86K) WATER (UNII: 059QF0KO0R) SODIUM HYDROXIDE (UNII: 55X04QC32I) STEARIC ACID (UNII: 4ELV7Z65AP) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0132-0079-00 100 in 1 JAR; Type 0: Not a Combination Product 11/01/1984 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC MONOGRAPH NOT FINAL part334 11/01/1984 04/30/2023 Labeler - C.B. Fleet Company, Inc. (003119054)