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Senna S

Contract Pharmacal Corp




FULL PRESCRIBING INFORMATION

GENTLE NATURAL VEGETABLE LAXATIVE

Compare to the Active Ingredients in Senokot-S®†

1000 Tablets

DO NOT USE IF IMPRINTED SAFETY SEAL UNDER CAP IS BROKEN OR MISSING

Drug Facts

(in each tablet)

Sennosides from Senna Concentrate 8.6 mg

Sodium Dioctylsulfosuccinate 50 mg

Laxative

Stool Softener

  • relieves occasional constipation (irregularity)
  • generally produces a bowel movement in 6-12 hours

Do not use

  • laxative products for longer than 1 week unless directed by a doctor
  • if you are now taking mineral oil, unless directed by a doctor.
  • stomach pain, nausea, vomiting, noticed a sudden change in bowel habits that continues over a period of 2 weeks.
  • you have rectal bleeding or fail to have a bowel movement after use of a laxative. These may indicate a serious condition.

ask a health care professional before use.

In case of overdose, get medical help or contact a Poison Control Center right away.

Directions take preferably at bedtime or as directed by a doctor.

age starting dosage maximum dosage
dults and children over 12 years 2 tablets once a day 4 tablets twice a day
children 6 to under 12 years 1 tablet once a day 2 tablets twice a day
children under 6 years ask a doctor

Other information store at room temperature, USP.

Inactive ingredients Croscarmellose Sodium, Dicalcium Phosphate, FD&C Yellow #5* Lake, FD&C Yellow #6 Lake, Hypromellose, Magnesium Silicate, Magnesium Stearate, Microcrystalline Cellulose, Mineral Oil, Polyethylene Glycol, Sodium Benzoate, Starch, Stearic Acid and Titanium Dioxide.

*Contains FD&C Yellow #5 Lake (Tartrazine) as a color additive.

†This product is not manufactured or distributed by Purdue Products L.P., owner of the registered trademark Senokot-S®.

Manufactured by:
Contract Pharmacal Corp.
135 Adams Avenue
Hauppauge, NY 11788 USA
www.cpc.com

Senna S

Senna S

Sennosides and Sodium Dioctylsulfosuccinate TABLET

Product Information

Product Type Human otc drug label Item Code (Source) NDC:10267-0490
Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
SENNA LEAF SENNA LEAF 8.5 mg
DOCUSATE SODIUM DOCUSATE 50 mg

Inactive Ingredients

Ingredient Name Strength
CROSCARMELLOSE SODIUM
DIBASIC CALCIUM PHOSPHATE DIHYDRATE
FD&C YELLOW NO. 5
FD&C YELLOW NO. 6
HYPROMELLOSES
magnesium silicate
MAGNESIUM STEARATE
cellulose, microcrystalline
LIGHT MINERAL OIL
polyethylene glycol 400
SODIUM BENZOATE
STARCH, CORN
STEARIC ACID
titanium dioxide

Product Characteristics

Color Size Imprint Code Shape
ORANGE 10 mm CPC;490 ROUND

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:10267-0490-7 60 in 1 BOTTLE
2 NDC:10267-0490-1 100 in 1 BOTTLE
3 NDC:10267-0490-4 1000 in 1 BOTTLE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part334 2001-06-05


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Be sure to consult your doctor before taking any medication!
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