DOCUSATE SODIUM capsule

国家: 美国

语言: 英文

来源: NLM (National Library of Medicine)

有效成分:

DOCUSATE SODIUM (UNII: F05Q2T2JA0) (DOCUSATE - UNII:M7P27195AG)

可用日期:

St. Marys Medical Park Pharmacy

INN（国际名称）:

DOCUSATE SODIUM

组成:

DOCUSATE SODIUM 100 mg

处方类型:

OTC DRUG

授权状态:

OTC monograph not final

产品特点

DOCUSATE SODIUM- DOCUSATE SODIUM CAPSULE
ST. MARYS MEDICAL PARK PHARMACY
_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._
----------
DOCUSATE SODIUM
ACTIVE INGREDIENT (IN EACH SOFTGEL)
Docusate sodium 100 mg
PURPOS E
Stool softener
US ES
prevents/relieves dry hard stool
results usually occurs 1 to 3 days after the first dose
WARNINGS
DO NOT USE
when abdominal pain, nausea, or vomiting are present
for more than one week unless directed by a doctor
ASK A DOCTOR BEFORE USE IF YOU
are taking mineral oil
have noticed a sudden change in bowel habits that last over 2 weeks
STOP USE AND ASK A DOCTOR IF
you have no bowel movement after 3 days
you have rectal bleeding
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
over 12
take 1-2 softgels daily until first
bowel movement; 1 softgel daily
years
thereafter
children 6 to 12 years
take 1 softgel daily
children under 6 years
consult a doctor
OTHER INFORMATION
TAMPER EVIDENT: DO NOT USE IF SAFETY SEAL UNDER CAP IS BROKEN OR
MISSING
store at room temperature 15
to 30
C (59
to 86
F)
protect from moisture
INACTIVE INGREDIENTS: D&C YELLOW # 10, FD&C RED # 40, GELATIN,
GLYCERIN, INK WHITE, POLYETHYLENE
GLYCOL, SORBITOL, PROPYLENE GLYCOL.
QUES TIONS ?
Adverse drug event call: [phone]
DOCUSATE SODIUM
ST MARYS PHARMACY
DOCUSATE SODIUM
docusate sodium capsule
PRODUCT INFORMATION
PRODUCT T YPE
HUMAN OTC DRUG
ITE M CODE (SOURCE )
NDC:6 0 76 0 -38 4(NDC:16 10 3-38 4)
ROUTE OF ADMINISTRATION
ORAL
ACTIVE INGREDIENT/ACTIVE MOIETY
INGREDIENT NAME
BASIS OF STRENGTH
STRE NG TH
DO CUSATE SO DIUM (UNII: F0 5Q2T2JA0 ) (DOCUSATE - UNII:M7P2719 5AG)
DOCUSATE SODIUM
10 0 mg
INACTIVE INGREDIENTS
o
o