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 overtake one 180 mg tablet with water once a day; do not take more than 1 tablet in 24 hours
children under 12 years of agedo not use
adults 65 years of age and olderask a doctor
consumers with kidney diseaseask 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 TypeHUMAN OTC DRUG LABELItem Code (Source)NDC:63824-926
Route of AdministrationORALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Fexofenadine Hydrochloride (Fexofenadine) Fexofenadine Hydrochloride180 mg
Inactive Ingredients
Ingredient NameStrength
silicon dioxide 
starch, corn 
croscarmellose sodium 
FD&C Red no. 40 
hypromelloses 
ferrosoferric oxide 
magnesium stearate 
mannitol 
polyethylene glycols 
powdered cellulose 
titanium dioxide 
Product Characteristics
ColorPINKScoreno score
ShapeOVALSize7mm
FlavorImprint Code 194;R
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:63824-926-051 in 1 CARTON
15 in 1 BLISTER PACK
2NDC:63824-926-101 in 1 CARTON
210 in 1 BLISTER PACK
3NDC:63824-926-303 in 1 CARTON
310 in 1 BLISTER PACK
4NDC:63824-926-404 in 1 CARTON
410 in 1 BLISTER PACK
5NDC:63824-926-802 in 1 CARTON
5NDC:63824-926-404 in 1 CARTON
510 in 1 BLISTER PACK
6NDC:63824-926-606 in 1 CARTON
610 in 1 BLISTER PACK
7NDC:63824-926-888 in 1 CARTON
710 in 1 BLISTER PACK
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
ANDAANDA07650201/02/2014
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