DOK- docusate sodium tablet

DOK by

Drug Labeling and Warnings

DOK by is a Otc medication manufactured, distributed, or labeled by REMEDYREPACK INC.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

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

Keep out of the 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 tablet as needed, not to exceed 3 tablets daily, or as directed by a doctor
• children under 12: consult a doctor
• tablets may be swallowed whole or crushed and mixed with food

Other information

• each tablet contains: calcium 50 mg, sodium 8 mg
• package not child resistant
• store at room temperature 15°C-30°C (59°F-86°F)
• Tamper Evident: Do not use if imprinted seal under cap is missing or broken

Inactive ingredients

cellulose, croscarmellose sodium, dicalcium phosphate, magnesium stearate, silica, stearic acid, talc

PRINCIPAL DISPLAY PANEL

DRUG: DOK

GENERIC: docusate sodium

DOSAGE: TABLET

ADMINSTRATION: ORAL

NDC: 70518-1983-0

COLOR: white

SHAPE: ROUND

SCORE: No score

SIZE: 11 mm

IMPRINT: GC422

PACKAGING: 30 in 1 BLISTER PACK

ACTIVE INGREDIENT(S):

• DOCUSATE SODIUM 100mg in 1

INACTIVE INGREDIENT(S):

• ANHYDROUS DIBASIC CALCIUM PHOSPHATE
• MAGNESIUM STEARATE
• SILICON DIOXIDE
• STEARIC ACID
• CROSCARMELLOSE SODIUM
• MICROCRYSTALLINE CELLULOSE
• TALC

INGREDIENTS AND APPEARANCE

DOK 
docusate sodium tablet

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 70518-1983(NDC:0904-6750)
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
Ingredient Name	Strength
STEARIC ACID (UNII: 4ELV7Z65AP)
CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)
MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)
ANHYDROUS DIBASIC CALCIUM PHOSPHATE (UNII: L11K75P92J)
MAGNESIUM STEARATE (UNII: 70097M6I30)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
TALC (UNII: 7SEV7J4R1U)

Product Characteristics
Color	white	Score	no score
Shape	ROUND	Size	11mm
Flavor		Imprint Code	GC422
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 70518-1983-0	30 in 1 BLISTER PACK; Type 0: Not a Combination Product	03/26/2017

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part334	03/26/2017

Labeler - REMEDYREPACK INC. (829572556)