GOOD SENSE MUCUS RELIEF- guaifenesin liquid
L Perrigo Company

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Perrigo Mucus Relief Drug Facts

Active ingredient (in each 5 mL tsp)

Guaifenesin, USP 100 mg

Purpose

Expectorant

Uses

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

Warnings

Ask a doctor before use if the child has

•: cough that occurs with too much phlegm (mucus)
•: persistent or chronic cough such as occurs with asthma

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.

Keep out of reach of children.

In case of overdose, get medical help or contact a Poison Control Center right away.

Directions

•: do not take more than 6 doses in any 24-hour period

Age	Dose
children 6 years to under 12 years	1-2 teaspoonfuls every 4 hours
children 4 years to under 6 years	½ - 1 teaspoonful every 4 hours
children under 4 years	do not use

Other information

•: each teaspoon contains: sodium 3 mg
•: store at 20°-25°C (68°-77°F)

Inactive ingredients

acesulfame potassium, citric acid, FD&C blue no. 1, FD&C red no. 40, flavor, glycerin, maltitol, propylene glycol, purified water, saccharin sodium, sodium benzoate, sorbitol solution, sucralose, xanthan gum

Questions or comments?
1-800-719-9260

Principal Display Panel

For Ages 4-12

SEE NEW DOSING DIRECTIONS

Children’s

Mucus Relief

Expectorant – Guaifenesin

Relieves Chest Congestion

Thins & Loosens Mucus

Alcohol Free

Grape Flavor Liquid

Compare to active ingredient of Mucinex® For Kids

GOOD SENSE MUCUS RELIEF
guaifenesin liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:0113-0288
Route of Administration	ORAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
GUAIFENESIN (UNII: 495W7451VQ) (GUAIFENESIN - UNII:495W7451VQ)	GUAIFENESIN	100 mg in 5 mL

Ingredient Name	Strength
Inactive Ingredients
ACESULFAME POTASSIUM (UNII: 23OV73Q5G9)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
FD&C RED NO. 40 (UNII: WZB9127XOA)
GLYCERIN (UNII: PDC6A3C0OX)
MALTITOL (UNII: D65DG142WK)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
WATER (UNII: 059QF0KO0R)
SACCHARIN SODIUM (UNII: SB8ZUX40TY)
SODIUM BENZOATE (UNII: OJ245FE5EU)
SORBITOL (UNII: 506T60A25R)
SUCRALOSE (UNII: 96K6UQ3ZD4)
XANTHAN GUM (UNII: TTV12P4NEE)

Product Characteristics
Color	PURPLE (clear)	Score
Shape		Size
Flavor	GRAPE	Imprint Code
Contains

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:0113-0288-26	1 in 1 CARTON	11/06/2007	10/15/2010
1		118 mL in 1 BOTTLE; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph final	part341	11/06/2007	10/15/2010

Labeler - L Perrigo Company (006013346)

Revised: 3/2018

Document Id: 441f09f7-7d36-45fc-a937-eb9658fd6a54

Set id: e0ca9979-4850-4ebd-be67-8883bb075cb6

Version: 2

Effective Time: 20180329

L Perrigo Company