MUCINEX ALLERGY- fexofenadine hydrochloride tablet 
RB Health (US) 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:

  • runny nose
  • itchy, watery eyes
  • sneezing
  • itching of the nose or throat

Warnings

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

Ask a doctor before use if you havekidney 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 ifan 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

  • safety sealed: do not use if carton is opened or if individual blister units are torn or opened
  • store between 20° and 25°C (68° and 77°F)
  • protect from excessive moisture
  • this product meets the requirements of USP Dissolution Test 2

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

10TABLETS 180 mg each

Principal Display Panel - 180 mg Blister Pack Carton
MUCINEX  ALLERGY
fexofenadine hydrochloride tablet
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:63824-926
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
FEXOFENADINE HYDROCHLORIDE (UNII: 2S068B75ZU) (FEXOFENADINE - UNII:E6582LOH6V) FEXOFENADINE HYDROCHLORIDE180 mg
Inactive Ingredients
Ingredient NameStrength
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 GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)  
POWDERED CELLULOSE (UNII: SMD1X3XO9M)  
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
Product Characteristics
ColorpinkScoreno score
ShapeOVALSize7mm
FlavorImprint Code 194;R
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:63824-926-051 in 1 CARTON01/02/201403/31/2018
15 in 1 BLISTER PACK; Type 0: Not a Combination Product
2NDC:63824-926-101 in 1 CARTON01/02/201403/31/2018
210 in 1 BLISTER PACK; Type 0: Not a Combination Product
3NDC:63824-926-303 in 1 CARTON01/02/201403/31/2018
310 in 1 BLISTER PACK; Type 0: Not a Combination Product
4NDC:63824-926-802 in 1 CARTON01/02/201403/31/2018
4NDC:63824-926-404 in 1 CARTON
410 in 1 BLISTER PACK; Type 0: Not a Combination Product
5NDC:63824-926-606 in 1 CARTON04/30/201403/31/2018
510 in 1 BLISTER PACK; Type 0: Not a Combination Product
6NDC:63824-926-888 in 1 CARTON04/30/201403/31/2018
610 in 1 BLISTER PACK; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
ANDAANDA07650201/02/201403/31/2018
Labeler - RB Health (US) LLC (081049410)

Revised: 7/2023
 
RB Health (US) LLC