Label: GLYCERIN- glycerin suppository
- NDC Code(s): 69842-722-25
- Packager: CVS Pharmacy
- 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.
Updated December 13, 2022
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- Active ingredient (in each suppository)
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 two weeks
- already used a laxative for more than 1 week
Stop use and consult a doctor if child has
- rectal bleeding
- no bowel movement within 1 hour of using this product
These symptoms may indicate a serious condition.
- Other information
- Inactive ingredients
- Pediatric Glycerin Suppositories, 25 count
INGREDIENTS AND APPEARANCE
Product Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69842-722 Route of Administration RECTAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength GLYCERIN (UNII: PDC6A3C0OX) (GLYCERIN - UNII:PDC6A3C0OX) GLYCERIN 1 g in 1.2 Inactive Ingredients Ingredient Name Strength SODIUM HYDROXIDE (UNII: 55X04QC32I) STEARIC ACID (UNII: 4ELV7Z65AP) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69842-722-25 25 in 1 JAR; Type 0: Not a Combination Product 08/18/2016 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part334 08/18/2016 Labeler - CVS Pharmacy (062312574) Registrant - DSC Laboratories Inc. (097807374) Establishment Name Address ID/FEI Business Operations DSC Laboratories Inc. 097807374 manufacture(69842-722)