MUCINEX MAXIMUM STRENGTH - guaifenesin tablet, extended release 
Reckitt Benckiser, Inc.

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MAXIMUM STRENGTH
Mucinex ®

Drug Facts

Active ingredient (in each extended-release bi-layer tablet)

Guaifenesin 1200 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

Do not use

Ask a doctor before use if you have

Stop use and ask a doctor if

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

Other information

Inactive ingredients

carbomer 934P, NF; FD&C blue #1 aluminum lake; hypromellose, USP; magnesium stearate, NF; microcrystalline cellulose, NF; sodium starch glycolate, NF

Questions?

1-866-MUCINEX (1-866-682-4639) You may also report side effects to this phone number.

Dist. by: Reckitt Benckiser Inc.
Parsippany, NJ 07054-0224

PRINCIPAL DISPLAY PANEL - 1200 mg Tablet Carton

MAXIMUM STRENGTH

NDC 63824-023-36

Mucinex®
1200 mg guaifenesin extended-release bi-layer tablets

EXPECTORANT

12
HOUR

Thins And Loosens Mucus
Relieves Chest Congestion

28 EXTENDED-RELEASE BI-LAYER TABLETS

PRINCIPAL DISPLAY PANEL - Tablet Carton

MUCINEX  MAXIMUM STRENGTH
guaifenesin   tablet, extended release
Product Information
Product Type HUMAN OTC DRUG NDC Product Code (Source) 63824-023
Route of Administration ORAL DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
Guaifenesin (Guaifenesin) Guaifenesin 1200 mg
Inactive Ingredients
Ingredient Name Strength
No Inactive Ingredients Found
Product Characteristics
Color WHITE (blue and white) Score no score
Shape OVAL Size 22mm
Flavor Imprint Code Mucinex;1200
Contains     
Packaging
# NDC Package Description Multilevel Packaging
1 63824-023-14 1 BOTTLE In 1 CARTON contains a BOTTLE
1 14 TABLET In 1 BOTTLE This package is contained within the CARTON (63824-023-14)
2 63824-023-36 4 BLISTER PACK In 1 CARTON contains a BLISTER PACK
2 7 TABLET In 1 BLISTER PACK This package is contained within the CARTON (63824-023-36)
3 63824-023-28 1 BOTTLE In 1 CARTON contains a BOTTLE
3 28 TABLET In 1 BOTTLE This package is contained within the CARTON (63824-023-28)
4 63824-023-43 1 BOTTLE In 1 BLISTER PACK contains a BOTTLE
4 42 TABLET In 1 BOTTLE This package is contained within the BLISTER PACK (63824-023-43)
5 63824-023-45 1 BOTTLE In 1 BLISTER PACK contains a BOTTLE
5 44 TABLET In 1 BOTTLE This package is contained within the BLISTER PACK (63824-023-45)

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
NDA NDA021282 08/11/2009

Labeler - Reckitt Benckiser, Inc. (094405024)
Revised: 12/2009 Reckitt Benckiser, Inc.