Label: KROGER STOOL SOFTENER FRUIT PUNCH- docusate sodium liquid
- NDC Code(s): 41226-714-08
- Packager: KROGER COMPANY
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated July 31, 2024
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- Official Label (Printer Friendly)
- Active ingredient (in each 5 mL)
- Purpose
- Uses
-
Warnings
Do not use
- laxative products for longer than 1 week unless directed by a doctor
Ask a doctor before use if you have
- stomach pain
- nausea
- vomiting
- noticed a sudden change in bowel habits that continues over a period of 2 weeks
Stop use and ask a doctor ifrectal 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
- must be given in a 6 to 8 oz glass of milk or fruit juice to prevent throat irritation
- may be taken as a single daily dose or in divided doses
- take maximum dose daily until first bowel movement, dosage should then be reduced according to individual response.
- do not exceed recommended dose
- 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
- Questions or comments?
-
Principal Display Panel
NDC 41226-714-08
Compare to the active ingredient in Colace® Clear*
Stool Softener Laxative
Docusate Sodium/ Stool SoftenerHelps gently relieves Constipation Overnight
Fruit Punch Flavor
Naturally and Artificially Flavor
8 FL OZ (237 mL)Package Contains One Bottle
Distributed by:
*This product is not manufactured or distributed by Avrio Health L.P., owner of the registered trademark Colace ®Clear.
IMPORTANT: Keep this carton for future reference on full labeling.
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INGREDIENTS AND APPEARANCE
KROGER STOOL SOFTENER FRUIT PUNCH
docusate sodium liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:41226-714 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 BENZYL ALCOHOL (UNII: LKG8494WBH) ANHYDROUS CITRIC ACID (UNII: XF417D3PSL) POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A) POVIDONE, UNSPECIFIED (UNII: FZ989GH94E) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) WATER (UNII: 059QF0KO0R) 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:41226-714-08 237 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 03/27/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M007 03/27/2023 Labeler - KROGER COMPANY (006999528)
