Country: Amerika Syarikat
Bahasa: Inggeris
Sumber: NLM (National Library of Medicine)
DOCUSATE SODIUM (UNII: F05Q2T2JA0) (DOCUSATE - UNII:M7P27195AG)
Reese Pharmaceutical Co
ORAL
OTC DRUG
Stool softener - relieves occasional constipation (irregularity) - generally produces a bowel movement in 12 to 72 hours
OTC monograph not final
PREFERRED STOOL SOFTENER LAXATIVE- DOCUSATE SODIUM CAPSULE, LIQUID FILLED REESE PHARMACEUTICAL CO _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._ ---------- DRUG FACTS ACTIVE INGREDIENT (IN EACH SOFTGEL) Docusate Sodium 250 mg PURPOSE Stool softener USES relieves occasional constipation (irregularity) generally produces a bowel movement in 12 to 72 hours WARNINGS DO NOT USE if you are presently taking mineral oil, unless told to do so by a doctor ASK A DOCTOR BEFORE USE IF YOU HAVE stomach pain nausea vomiting noticed a sudden change in bowel movements that lasts over 2 weeks STOP USE AND ASK A DOCTOR IF you have rectal bleeding or fail to have a bowel movement after use of a laxative. These could be signs of a serious condition. you need to use a stool softener laxative for more than 1 week IF PREGNANT OR BREAST-FEEDING, ask a health professional before use. KEEP OUT OF REACH OF CHILDREN. In case of overdose, get medical help or contact a Poison Control Center right away. DIRECTIONS Take only by mouth. Doses may be taken as a single daily dose or in divided doses. adults and children 12 years and over take 1 to 3 softgels daily children 2 to under 12 years of age take 1 softgel daily children under 2 years ask a doctor OTHER INFORMATION each softgel contains: sodium 7 mg store at room temperature 15° to 30°C (59° to 86°F) INACTIVE INGREDIENTS FD&C RED #40, FD&C YELLOW #6, GELATIN, GLYCEROL, POLYETHYLENE GLYCOL, PURIFIED WATER, SORBITOL. PREFERRED STOOL SOFTENER LAXATIVE docusate sodium capsule, liquid filled PRODUCT INFORMATION PRODUCT TYPE HUMAN OTC DRUG ITEM CODE (SOURCE) NDC:10956-781 ROUTE OF ADMINISTRATION ORAL ACTIVE INGREDIENT/ACTIVE MOIETY INGREDIENT NAME BASIS OF STRENGTH STRENGTH DOCUSATE SODIUM (UNII: F05Q2T2JA0) (DOCUSATE - UNII:M7P27195AG) DOCUSATE SODIUM 250 mg INACTIVE INGREDIENTS Reese Pharmaceutical Co INGREDIENT NAME STRENGTH FD&C Baca dokumen lengkap