Mucus Relief description, usages, side effects, indications, overdosage, supplying and lots more!

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Mucus Relief

Major Pharmaceuticals

Major 44-532


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Active ingredient(s)

 Guaifenesin 400 mg

Purpose

 Expectorant

Use(s)

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

Warnings

Ask a doctor before use if you have

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

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 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

  • take with a full glass of water
  • adults and children 12 years of age and over: 1 tablet, every 4 hours. Do not take more than 6 tablets in 24 hours.
  • children under 12 years: do not use 

Mucus Relief Other information

  • store at controlled room temperature 15º-30ºC (59º-86ºF)
  • see end flap for expiration date and lot number

Inactive ingredients

FD&C blue #1 alluminum lake, hypromellose, magnesium stearate, maltodextrin, microcrystalline cellulose, polyethylene glycol, povidone, silicon dioxide, sodium starch glycolate, stearic acid

Questions?

 To Report Adverse Drug Event Call: (800) 616-2471

Principal Display Panel

NDC 0904-5758-46

MAJOR®

MucusRelief

Guaifenesin 400 mg

Expectorant

• Alleviates Chest Congestion

• Loosens Mucus

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

50844     REV0510E53201    M-17

Distributed by Major Pharmaceuticals

31778 Enterprise Drive

Livonia, MI 48150 USA

Re-order No. 100264        Rev. 10/10

Mucus Relief

Mucus Relief

Guaifenesin TABLET

Product Information

Product Type Human otc drug label Item Code (Source) NDC:0904-5758
Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
Guaifenesin GUAIFENESIN 400 mg

Inactive Ingredients

Ingredient Name Strength
FD&C BLUE NO. 1
HYPROMELLOSES
MAGNESIUM STEARATE
maltodextrin
cellulose, microcrystalline
povidone
SILICON DIOXIDE
SODIUM STARCH GLYCOLATE TYPE A POTATO

Product Characteristics

Color Size Imprint Code Shape
BLUE 13 mm 44;532 ROUND

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 30 in 1 BOTTLE, PLASTIC
2 NDC:0904-5758-01 1 in 1 CARTON

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part341 2005-12-22


PLEASE, BE CAREFUL!
Be sure to consult your doctor before taking any medication!
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