STOOL SOFTENER- docusate sodium capsule, liquid filled

Valsts: Amerikas Savienotās Valstis

Valoda: angļu

Klimata pārmaiņas: NLM (National Library of Medicine)

Aktīvā sastāvdaļa:

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

Pieejams no:

Geri-Care Pharmaceutical Corp

Ievadīšanas:

ORAL

Receptes veids:

OTC DRUG

Ārstēšanas norādes:

Stool Softener - relieves occasional constipation (irregularity) - generally produces bowel movement in 12 to 72 hours

Autorizācija statuss:

OTC monograph not final

Produkta apraksts

STOOL SOFTENER- DOCUSATE SODIUM CAPSULE, LIQUID FILLED
GERI-CARE PHARMACEUTICAL CORP
----------
GC425 (426)
ACTIVE INGREDIENT (IN EACH SOFTGEL)
Docusate Sodium 250 mg
PURPOSE
Stool Softener
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
adults and children 12 years and older: take 1 softgel daily or as
directed by a doctor
children under 12: do not use
do not exceed recommended dose
OTHER INFORMATION
each softgel contains: SODIUM 15 MG
store at 59°-77°F (15°-25°C)
keep tightly closed
product of Romania
Package not child resistant
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, glycerol, PEG,
purified water,
sorbitol special
QUESTIONS OR COMMENTS?
1-800-540-3765
PACKAGE LABEL
STOOL SOFTENER
docusate sodium capsule, liquid filled
PRODUCT INFORMATION
PRODUCT TYPE
HUMAN OTC DRUG
ITEM CODE (SOURCE)
NDC:57896-426
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
INGREDIENT NAME
STRENGTH
GELATIN (UNII: 2G86QN327L)
GLYCERIN (UNII: PDC6A3C0OX)
Geri-Care Pharmaceutical Corp
FD&C YELLOW NO. 6 (UNII: H77VEI93A8)
WATER (UNII: 059QF0KO0R)
FD&C RED NO. 40 (UNII: WZB9127XOA)
POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)
SORBITOL (UNII: 506T60A25R)