দেশ: মার্কিন যুক্তরাষ্ট্র
ভাষা: ইংরেজি
সূত্র: NLM (National Library of Medicine)
DOCUSATE SODIUM (UNII: F05Q2T2JA0) (DOCUSATE - UNII:M7P27195AG)
NuCare Pharmaceuticals,Inc.
ORAL
OTC DRUG
Stool Softener Laxative - relieves occasional constipation (irregularity) - generally produces bowel movement in 12 to 72 hours
OTC monograph not final
DOCUSATE SODIUM- DOCUSATE SODIUM CAPSULE, LIQUID FILLED NUCARE PHARMACEUTICALS,INC. _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._ ---------- GC 401 ACTIVE INGREDIENT (IN EACH SOFTGEL) Docusate Sodium 100 mg PURPOSE Stool Softener Laxative USES relieves occasional constipation (irregularity) generally produces bowel movement in 12 to 72 hours WARNINGS ASK A DOCTOR BEFORE USE IF YOU • have stomach pain, nausea or vomiting • have a sudden change in bowel habits that persists over a period of 2 weeks • are presently taking mineral oil STOP USE AND ASK A DOCTOR IF • you need to use a laxative longer than 1 week • you have rectal bleeding or fail to have a bowel movement. These could be signs of a serious condition. 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 • do not exceed recommended dose • adults and children 12 years and older: take 1-3 softgels daily until first bowel movement; 1 softgel daily thereafter, or as directed by a doctor • children under 12: consult a doctor OTHER INFORMATION • EACH SOFTGEL CONTAINS: sodium 7 mg. Very low sodium • store at 59°-77°F (15°-25°C) • keep tightly closed • TAMPER EVIDENT: Do not use if imprinted seal under cap is missing or broken. INACTIVE INGREDIENTS FD&C red #40, FD&C yellow #6 (sunset yellow), gelatin, glycerin, PEG, sorbitol special, water. PACKAGE LABEL DOCUSATE SODIUM docusate sodium capsule, liquid filled PRODUCT INFORMATION PRODUCT TYPE HUMAN OTC DRUG ITEM CODE (SOURCE) NDC:68071-2874(NDC:57896-401) ROUTE OF ADMINISTRATION ORAL ACTIVE INGREDIENT/ACTIVE MOIETY INGREDIENT NAME BASIS OF STRENGTH STRENGTH DOCUSATE SODIUM (UNII: F05Q2T2JA0) (DOCUSATE - UNII:M7P27195AG) DOCUSATE SODIUM 100 mg INACTIVE INGREDIENTS NuCare Pharmaceuticals সম্পূর্ণ নথি পড়ুন