Label: GLYCERIN suppository
- NDC Code(s): 70000-0429-1
- Packager: Cardinal Health
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 12, 2024
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- 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 formore than 1 week
- Directions - single daily dose
- Other information
- Inactive ingredients
- Questions or comments?
- Label
-
INGREDIENTS AND APPEARANCE
GLYCERIN
glycerin suppositoryProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:70000-0429 Route of Administration RECTAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength GLYCERIN (UNII: PDC6A3C0OX) (GLYCERIN - UNII:PDC6A3C0OX) GLYCERIN 1 g 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:70000-0429-1 25 in 1 JAR; Type 0: Not a Combination Product 01/02/2019 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M007 01/02/2019 Labeler - Cardinal Health (063997360) Registrant - DSC Laboratories, Inc. (097807374) Establishment Name Address ID/FEI Business Operations DSC Laboratories, Inc. 097807374 manufacture(70000-0429)