MUCINEX  ALLERGY- fexofenadine hydrochloride tablet 
Reckitt Benckiser LLC

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Mucinex®
Allergy

Drug Facts

Active ingredient (in each tablet)

Fexofenadine HCl USP, 180 mg

Purpose

Antihistamine

Uses

temporarily relieves these symptoms due to hay fever or other upper respiratory allergies:

Warnings

Do not use if you have ever had an allergic reaction to this product or any of its ingredients.

Ask a doctor before use if you have kidney disease. Your doctor should determine if you need a different dose.

When using this product

  • do not take more than directed
  • do not take at the same time as aluminum or magnesium antacids
  • do not take with fruit juices (see Directions)

Stop use and ask a doctor if an allergic reaction to this product occurs. Seek medical help right away.

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

adults and children 12 years of age and over take one 180 mg tablet with water once a day; do not take more than 1 tablet in 24 hours
children under 12 years of age do not use
adults 65 years of age and older ask a doctor
consumers with kidney disease ask a doctor

Other information

Inactive ingredients

colloidal silicon dioxide, corn starch, croscarmellose sodium, FD&C Red no. 40, hypromellose, iron oxide black, magnesium stearate, mannitol, polyethylene glycol, powder cellulose and titanium dioxide

Questions?

Call 1-855-419-9622

Dist. By Reckitt Benckiser
Parsippany, NJ 07054-0224
Made in India

PRINCIPAL DISPLAY PANEL - 180 mg Blister Pack Carton

NEW

NDC 63824-926-10

NON-DROWSY
Mucinex®
ALLERGY

Fexofenadine Hydrochloride Tablets USP, 180 mg/Antihistamine

INDOOR & OUTDOOR ALLERGY RELIEF

24hr

ORIGINAL
PRESCRIPTION STRENGTH

✓ Sneezing
✓ Runny Nose
✓ Itchy, Watery Eyes
✓ Itchy Nose or Throat

10 TABLETS 180 mg each

Principal Display Panel - 180 mg Blister Pack Carton
MUCINEX   ALLERGY
fexofenadine hydrochloride tablet
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:63824-926
Route of Administration ORAL DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
Fexofenadine Hydrochloride (UNII: 2S068B75ZU) (Fexofenadine - UNII:E6582LOH6V) Fexofenadine Hydrochloride 180 mg
Inactive Ingredients
Ingredient Name Strength
silicon dioxide (UNII: ETJ7Z6XBU4)  
starch, corn (UNII: O8232NY3SJ)  
croscarmellose sodium (UNII: M28OL1HH48)  
FD&C Red no. 40 (UNII: WZB9127XOA)  
hypromelloses (UNII: 3NXW29V3WO)  
ferrosoferric oxide (UNII: XM0M87F357)  
magnesium stearate (UNII: 70097M6I30)  
mannitol (UNII: 3OWL53L36A)  
polyethylene glycols (UNII: 3WJQ0SDW1A)  
powdered cellulose (UNII: SMD1X3XO9M)  
titanium dioxide (UNII: 15FIX9V2JP)  
Product Characteristics
Color PINK Score no score
Shape OVAL Size 7mm
Flavor Imprint Code 194;R
Contains     
Packaging
# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:63824-926-05 1 in 1 CARTON
1 5 in 1 BLISTER PACK
2 NDC:63824-926-10 1 in 1 CARTON
2 10 in 1 BLISTER PACK
3 NDC:63824-926-30 3 in 1 CARTON
3 10 in 1 BLISTER PACK
4 NDC:63824-926-40 4 in 1 CARTON
4 10 in 1 BLISTER PACK
5 NDC:63824-926-80 2 in 1 CARTON
5 NDC:63824-926-40 4 in 1 CARTON
5 10 in 1 BLISTER PACK
6 NDC:63824-926-60 6 in 1 CARTON
6 10 in 1 BLISTER PACK
7 NDC:63824-926-88 8 in 1 CARTON
7 10 in 1 BLISTER PACK
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA076502 01/02/2014
Labeler - Reckitt Benckiser LLC (094405024)

Revised: 4/2014
Document Id: b87ef385-cbb8-41ae-9cef-e4bf9af038f4
Set id: 822a1976-97fa-44c6-b12b-f8239af63adf
Version: 2
Effective Time: 20140428
 
Reckitt Benckiser LLC