Purpose

Laxative

Uses

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

Warnings

Do not use

laxative products for longer than 1 week unless directed by a doctor

Aska doctor before use if you have

stomach pain
nausea
vomiting
noticed a sudden change in bowel habits that continues overa period of 2 weeks

Stop use and ask a doctorif you have rectal bleeding or fail to have a bowel movementafter use of a laxative. These may indicate 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 ControlCenter right away.

Directions

take preferably at bedtime or as directed by a doctor

age	starting dosage	maximum dosage
adults and children 12 years of age and over	2 tablets oncea day	4 tablets twicea day
children 6 to under12 years	1 tablet once aday	2 tablets twicea day
children 2 to under6 years	1/2 tablet oncea day	1 tablet twicea day
children under2 years	ask a doctor	ask a doctor

Other Information

each tablet contains: calcium 20 mg
store at 25°C (77°F); excursions permitted between 15°-30°C (59°-86°F)

Inactive ingredients

croscarmellose sodium, dicalciumphosphate, hypromellose, magnesium stearate, maltodextrin, microcrystallinecellulose, mineral oil, polyethylene glycol, talc

Avrio Health L.P.

305616-0B

50 Tablets
NDC 67618-300-50

100 Tablets
NDC 67618-300-10

SENOKOT
standardized senna concentrate tablet

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:67618-300
Route of Administration	ORAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
SENNOSIDES (UNII: 3FYP5M0IJX) (SENNOSIDES - UNII:3FYP5M0IJX)	SENNOSIDES	8.6 mg

Ingredient Name	Strength
Inactive Ingredients
CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)
CALCIUM PHOSPHATE, DIBASIC, ANHYDROUS (UNII: L11K75P92J)
HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)
MAGNESIUM STEARATE (UNII: 70097M6I30)
MALTODEXTRIN (UNII: 7CVR7L4A2D)
CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
MINERAL OIL (UNII: T5L8T28FGP)
POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)
TALC (UNII: 7SEV7J4R1U)

Product Characteristics
Color	BROWN	Score	no score
Shape	ROUND	Size	9mm
Flavor		Imprint Code	S
Contains

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:67618-300-20	2 in 1 CARTON	06/01/1956
1		10 in 1 BLISTER PACK; Type 0: Not a Combination Product
2	NDC:67618-300-50	1 in 1 CARTON	06/01/1956
2		50 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
3	NDC:67618-300-10	1 in 1 CARTON	06/01/1956
3		100 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC Monograph Drug	M007	06/01/1956

Labeler - Atlantis Consumer Healthcare, Inc. (118983925)

Registrant - Atlantis Consumer Healthcare, Inc. (118983925)

Senokot (standardized senna concentrate)

Purpose

Senokot
(standardized senna concentrate)