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

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Mucus Relief Chest

Rite Aid

Rite Aid 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 or bothersome mucus and make coughs more productive

Warnings

Ask a doctor before use if you have

  • cough tha 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 Chest Other information

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

Inactive ingredients

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

Principal Display Panel

Mucus Relief Chest

RITE

AID®

PHARMACY

Guaifenesin 400 mg

Mucus Relief

Chest

Exopectorant

Immediate-release

Relieves Chest Congestion

Thins And Loosens Mucus

TAMPER EVIDENT: DO NOT USE IF CARTON IS OPENED OR IF BLISTER UNIT IS TORN, BROKEN OR SHOWS ANY SIGNS OF TAMPERING

50844      ORG051043203

DISTRIBUTED BY:

Rite Aid

30 Hunter Lane, Camp Hill, PA 17011

Mucus Relief Chest

Guaifenesin TABLET, COATED

Product Information

Product Type Human otc drug label Item Code (Source) NDC:11822-0532
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
polyethylene glycol
povidone
SILICON DIOXIDE
SODIUM STARCH GLYCOLATE TYPE A POTATO
STEARIC ACID

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 10 in 1 BLISTER PACK
2 NDC:11822-0532-3 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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