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Guaifenesin 1200 mg (guaifenesin 1200 mg) Dailymed


Generic: guaifenesin 1200 mg is used for the treatment of Bronchitis Common Cold Cough Laryngitis Pharyngitis Rhinitis, Allergic, Perennial Sinusitis Whooping Cough


IMPRINT: 41     SHAPE: oval
    COLOR: blue

All Imprints

guaifenesin 1200 mg - 41 oval blue

guaifenesin 600 mg - 42 oval blue

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Otc - Active Ingredient Section


For 600 mg:             Active ingredient (in each extended-release tablet)

Guaifenesin, USP 600 mg

For 1200 mg: Active ingredient (in each extended-release tablet)

Guaifenesin, USP 1200 mg

Otc - Purpose Section


Purpose


Expectorant

Indications & Usage Section


Uses


• helps loosen phlegm (mucus) and thin bronchial secretions to rid the bronchial passageways of bothersome mucus and make coughs more productive

Warnings Section


Otc - Do Not Use Section


Do not use

• for children under 12 years of age

Otc - Ask Doctor Section


Ask a doctor before use if you have

• persistent or chronic cough such as occurs with smoking, asthma, chronic bronchitis, or emphysema • cough accompanied by too much phlegm (mucus)

Otc - Stop Use Section


Stop use and ask a doctor if
  • cough lasts more than 7 days, comes back, or occurs with fever, rash, or persistent headache. These could be signs of a serious illness.

Otc - Pregnancy Or Breast Feeding Section


If pregnant or breast-feeding, ask a health professional before use.

Otc - Keep Out Of Reach Of Children Section


Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center (1-800-222-1222) right away.

Dosage & Administration Section


Directions

For 600 mg

• do not crush, chew, or break extended - release tablet • take with a full glass of water • this product can be administered without regard for the timing of meals • adults and children 12 years of age and over: 1 or 2 extended - release tablets every 12 hours. Do not exceed 4 extended - release tablets in 24 hours. • children under 12 years of age: do not use

For 1200 mg

• do not crush, chew, or break extended - release tablet • take with a full glass of water • this product can be administered without regard for the timing of meals • adults and children 12 years of age and over: 1 extended - release tablet every 12 hours. Do not exceed 2 extended - release tablets in 24 hours. • children under 12 years of age: do not use

Storage And Handling Section


Other information


• store at 20-25°C (68-77°F)

Inactive Ingredient Section


Inactive ingredients
colloidal silicon dioxide, copovidone, FD&C Blue No. 1 Aluminum lake, hypromellose, magnesium stearate, maltodextrin, microcrystalline cellulose, povidone (K-30), sodium starch glycolate, stearic acid

Otc - Questions Section


Questions or comments?

Call 1-877-376-4271 (weekdays 9 AM to 5 PM) You may also report side effects to this phone number.

Manufactured for: Time-Cap Labs, Inc. 7 Michael Avenue, Farmingdale, NY 11735, USA

Manufactured by: Marksans Pharma Ltd. Plot No. L-82, L-83 Verna Indl. Estate Verna, Goa-403722, India 

Principal Display Panel


NDC: 25000-042-55

Guaifenesin Extended-Release Tablets 600 mg

20's count (2 x 10's buler) Carton

NDC: 25000-042-01

Guaifenesin Extended-Release Tablets 600 mg

20's count Bottle Label

NDC: 25000-042-01

Guaifenesin Extended-Release Tablets 600 mg

20's count Bottle Carton

NDC: 25000-042-12

Guaifenesin Extended-Release Tablets 600 mg

500's count Bottle Label

NDC: 25000-041-75

Guaifenesin Extended-Release Tablets 1200 mg

12's count (2 x 6's buler) Carton

NDC: 25000-041-12

Guaifenesin Extended-Release Tablets 1200 mg

500's count Bottle Label

DISCLAIMER:

"This tool does not provide medical advice, and is for informational and educational purposes only, and is not a substitute for professional medical advice, treatment or diagnosis. Call your doctor to receive medical advice. If you think you may have a medical emergency, please dial 911."

"Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. We may limit or otherwise restrict your access to the API in line with our Terms of Service."

"This product uses publicly available data from the U.S. National Library of Medicine (NLM), National Institutes of Health, Department of Health and Human Services; NLM is not responsible for the product and does not endorse or recommend this or any other product."

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