CHILDREN ALLERGY- fexofenadine hcl suspension 
Walgreens

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DRUG FACTS

Active ingredient (in each 5 mL)

Fexofenadine HCl, USP 30 mg

Purpose

Antihistamine

Uses

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

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

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 (1-800-222-1222) right away.

Direction

  • shake well before using
  • use only with enclosed dosing cup
adults and children 12 years of age and overtake 10 mL every 12 hours; do not take more than 20 mL in 24 hours
children 2 to under 12 years of agetake 5 mL every 12 hours; do not take more than 10 mL in 24 hours
children under 2 years of ageask a doctor
adults 65 years of age and olderask a doctor
consumers with kidney diseaseask a doctor

Note: mL = milliliters

Other information

  • each 5 mL contains: sodium 17 mg
  • store between 20º to 25ºC (68º and 77ºF)
  • before using any medication, read all label directions. Keep carton, it contains important information.

Inactive ingredients

artificial raspberry flavor, butylparaben, edetate disodium, poloxamer 407, propylene glycol, propylparaben, purified water, sodium phosphate dibasic, sodium phosphate monobasic, sucrose, titanium dioxide, xanthan gum, xylitol

Questions or comments?

Call 1-877-753-3935 Monday-Friday 9AM-5PM EST

Principal Display Panel

Compare to the active ingredient in Children's Allegra® Allergy††

NON-DROWSY

2 YEARS & OLDER

Children's Allergy Relief

FEXOFENADINE HCl ORAL SUSPENSION

30 mg/ 5 mL/ ANTIHISTAMINE

Dye Free  Non-Drowsy

12-Hour Relief  Alcohol Free

  • Indoor/outdoor allergy relief of sneezing, runny nose, itchy nose or throat & itchy, watery eyes

AGES 2 YEARS & OLDER

BERRY FLAVOR

FL OZ (mL)

LIQUID ORAL SUSPENSION

USE ONLY WITH ENCLOSED DOSING CUP. WASH AND LET AIR DRY AFTER EACH USE

*This product is not manufactured or distributed by Chattem Inc., distributor of Children's Allegra® Allergy.

TAMPER EVIDENT: DO NOT USE IF CARTON, UNPRINTED FOIL INNER SEAL OR NECKBAND PRINTED WITH "SEAL FOR YOUR PROTECTION" IS OPENED, TORN OR MISSING.

KEEP OUTER CARTON FOR COMPLETE WARNINGS AND PRODUCT INFORMATION .

DISTRIBUTED BY: WALGREEN CO.

DEERFIELD, IL 60015

Product Label

Fexofenadine HCl, USP 30 mg

WALGREENS Children's Allergy Relief Berry Flavor

CHILDREN ALLERGY 
fexofenadine hcl suspension
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0363-2600
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
FEXOFENADINE HYDROCHLORIDE (UNII: 2S068B75ZU) (FEXOFENADINE - UNII:E6582LOH6V) FEXOFENADINE HYDROCHLORIDE30 mg  in 5 mL
Inactive Ingredients
Ingredient NameStrength
BUTYLPARABEN (UNII: 3QPI1U3FV8)  
EDETATE DISODIUM (UNII: 7FLD91C86K)  
POLOXAMER 407 (UNII: TUF2IVW3M2)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
PROPYLPARABEN (UNII: Z8IX2SC1OH)  
WATER (UNII: 059QF0KO0R)  
SODIUM PHOSPHATE, DIBASIC, ANHYDROUS (UNII: 22ADO53M6F)  
SODIUM PHOSPHATE, MONOBASIC, ANHYDROUS (UNII: KH7I04HPUU)  
SUCROSE (UNII: C151H8M554)  
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
XANTHAN GUM (UNII: TTV12P4NEE)  
XYLITOL (UNII: VCQ006KQ1E)  
Product Characteristics
Color    Score    
ShapeSize
FlavorBERRYImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:0363-2600-041 in 1 BOX10/31/2023
1118 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
2NDC:0363-2600-081 in 1 BOX10/31/2023
2237 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
ANDAANDA20333010/31/2023
Labeler - Walgreens (008965063)

Revised: 10/2023
 
Walgreens