Label: WALGREENS ADULT GLYCERIN LAXATIVE- glycerin suppository suppository
- NDC Code(s): 0363-0445-00
- Packager: Walgreens
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated February 6, 2024
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- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active Ingredient
- Uses
- Warnings
- Do not use
- Ask a doctor before use if you have
- When using this product
- Stop use and ask a doctor if
- If pregnant or breast-feeding,
- Keep out of reach of children.
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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 Walgreens Infants & Children suppositories
children under 2 years ask a doctor-Insert 1 suppository well up into the rectum and retain for 15 minutes
-It need not melt to produce laxative action - Other information
- Inactive ingredients
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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 Walgreens Infants & Children suppositories
children under 2 years ask a doctor
-Insert 1 suppository well up into the rectum and retain for 15 minutes
-It need not melt to produce laxative action - Product Label
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INGREDIENTS AND APPEARANCE
WALGREENS ADULT GLYCERIN LAXATIVE
glycerin suppository suppositoryProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0363-0445 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 STEARIC ACID (UNII: 4ELV7Z65AP) SODIUM HYDROXIDE (UNII: 55X04QC32I) WATER (UNII: 059QF0KO0R) Product Characteristics Color white (CLEAR) Score Shape BULLET Size 32mm Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0363-0445-00 100 in 1 JAR; Type 0: Not a Combination Product 10/28/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M007 10/06/2014 Labeler - Walgreens (008965063) Registrant - Unipack LLC (116015769) Establishment Name Address ID/FEI Business Operations Unipack LLC 009248480 manufacture(0363-0445)