CHEST CONGESTION RELIEF- guaifenesin tablet

Chest Congestion Relief by

Drug Labeling and Warnings

Chest Congestion Relief by is a Otc medication manufactured, distributed, or labeled by Meijer, Inc., Geri-Care Pharmaceuticals, Corp. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient (in each caplet)

Guaifenesin 400 mg

Purpose

Expectorant

Uses

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

Warnings

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 excessive phlegm (mucus)

Stop use and ask a doctor if

• cough lasts more than 7 days or comes back
• cough occurs with fever, rash or persistent headache
• these could be signs of a serious illness.

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 full glass of water
• not intended for use in children under 12 years of age

• adults and children 12 years of age and over: take 1 caplet, every 4 hours, ; while symptoms persist do ; not exceed 6 doses in 24 hours
• children under 12 years of age: do not use

Other information

Tamper Evident: do not use if imprinted safety seal under cap is broken or missing.

store at room temperature 15°-30°C (59°-86°F)

Inactive ingredients

cellulose, magnesium stearate, maltodextrin, povidone, silica, stearic acid.

Questions or comments?

1-800-540-3765

package Label

INGREDIENTS AND APPEARANCE

CHEST CONGESTION RELIEF 
guaifenesin tablet

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 79481-0714
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
GUAIFENESIN (UNII: 495W7451VQ) (GUAIFENESIN - UNII:495W7451VQ)	GUAIFENESIN	400 mg

Inactive Ingredients
Ingredient Name	Strength
CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
MAGNESIUM STEARATE (UNII: 70097M6I30)
MALTODEXTRIN (UNII: 7CVR7L4A2D)
POVIDONE (UNII: FZ989GH94E)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
STEARIC ACID (UNII: 4ELV7Z65AP)

Product Characteristics
Color	white	Score	2 pieces
Shape	OVAL	Size	17mm
Flavor		Imprint Code	AP;152
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 79481-0714-5	50 in 1 BOTTLE; Type 0: Not a Combination Product	03/01/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M012	03/01/2025

Labeler - Meijer, Inc. (006959555)

Registrant - Geri-Care Pharmaceuticals, Corp (611196254)