Label: WALGREENS STOOL SOFTENER FRUIT PUNCH- docusate sodium liquid
- NDC Code(s): 0363-7140-08
- Packager: WALGREENS CO.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated November 11, 2024
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- Official Label (Printer Friendly)
- Active ingredient (in each 5 mL)
- Purpose
- Uses
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Warnings
Do not use
- ▪
- laxative products for longer than 1 week unless directed by a doctor
Ask a doctor before use if you have
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- stomach pain
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- nausea
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- vomiting
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- noticed a sudden change in bowel habits that continues over a period of 2 weeks
Stop use and ask a doctor if you have rectal bleeding of fail to have a bowel movement after use of laxative. These may indicate a serious condition.
- PREGNANCY OR BREAST FEEDING
- KEEP OUT OF REACH OF CHILDREN
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Directions
- •
- follow dosing directions below or take as directed by doctor
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- must be given in a 6 to 8 oz glass of milk or fruit juice to prevent throat irritation
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- may be taken as a single daily dose or in divided doses
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- take maximum dose daily until first bowel movement, dosage should then be reduced according to individual response.
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- do not exceed recommended dose
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- shake well before using
Age
Dose
Adults and children 12 years and over
5 mL-30 mL
Children 2 to under 12 years
5 mL-15 mL
- Other information
- Inactive ingredients
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Principal Display Panel
NDC 0363-7140-08
Compare to Colace® Clear active ingredient††
Walgreens
Stool Softener
DOCUSATE SODIUM 50 MG/5 ML STOOL SOFTENERLIQUID
Effective relief of occasional constipation
FRUIT PUNCH FLAVOR
NATURALLY AND ARTIFICIALLY FLAVOR
8 FL OZ (237 mL)Package Contains One Bottle
DISTRIBUTED BY: WALGREEN CO.
200 WILMOT RD., DEERFIELD, IL 60015
Walgreens 100 % SATISFACTION GUARANTEED
Walgreens.com © 2017 walgreen.com
†Walgreens Pharmacist Survey
*This product is not manufactured or distributed by Purdue Products L.P., owner of the registered trademark COLACE®.
IMPORTANT: Keep this carton for future reference on full labeling.
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INGREDIENTS AND APPEARANCE
WALGREENS STOOL SOFTENER FRUIT PUNCH
docusate sodium liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0363-7140 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength DOCUSATE SODIUM (UNII: F05Q2T2JA0) (DOCUSATE - UNII:M7P27195AG) DOCUSATE SODIUM 50 mg in 5 mL Inactive Ingredients Ingredient Name Strength ANHYDROUS CITRIC ACID (UNII: XF417D3PSL) POTASSIUM SORBATE (UNII: 1VPU26JZZ4) POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A) POVIDONE, UNSPECIFIED (UNII: FZ989GH94E) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) WATER (UNII: 059QF0KO0R) SODIUM BENZOATE (UNII: OJ245FE5EU) SODIUM CITRATE, UNSPECIFIED FORM (UNII: 1Q73Q2JULR) SORBITOL (UNII: 506T60A25R) SUCRALOSE (UNII: 96K6UQ3ZD4) XANTHAN GUM (UNII: TTV12P4NEE) Product Characteristics Color Score Shape Size Flavor FRUIT PUNCH Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0363-7140-08 237 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 04/25/2019 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M007 04/25/2019 Labeler - WALGREENS CO. (008965063)