Label: GLYCERIN- glycerin suppository
- NDC Code(s): 63868-282-25
- Packager: Chain Drug Marketing Association Inc.
- Category: HUMAN OTC DRUG LABEL
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.
Drug Label Information
Updated December 13, 2022
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- Official Label (Printer Friendly)
- Active ingredient (in each suppository)
- Purpose
- Uses
-
Warnings
For rectal use only
May cause rectal discomfort or a burning sensation
Ask a Doctor before using any laxative if child has
- 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
- Directions
- Other information
- Inactive ingredients
- Pediatric Glycerin Suppositories, 25 count
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INGREDIENTS AND APPEARANCE
GLYCERIN
glycerin suppositoryProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:63868-282 Route of Administration RECTAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength GLYCERIN (UNII: PDC6A3C0OX) (GLYCERIN - UNII:PDC6A3C0OX) GLYCERIN 1.2 g Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) SODIUM HYDROXIDE (UNII: 55X04QC32I) STEARIC ACID (UNII: 4ELV7Z65AP) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:63868-282-25 25 in 1 JAR; Type 0: Not a Combination Product 03/20/2012 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part334 03/20/2012 Labeler - Chain Drug Marketing Association Inc. (011920774) Registrant - DSC Laboratories Inc. (097807374) Establishment Name Address ID/FEI Business Operations DSC Laboratories Inc. 097807374 manufacture(63868-282)