CHILDRENS ALLERGY RELIEF- fexofenadine hydrochloride suspension 
Kroger Company

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Childrens Allergy Fexofenadine Hydrochloride Oral Suspension

Drug Facts

Active ingredient

(in each 5 mL = 1 teaspoonful)
Fexofenadine HCl, USP 30 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 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

  • shake well before using
  • use only with enclosed dosing cup
 adults and children 12 years of age and over take 2 teaspoonfuls (10 mL) every 12 hours; do not take more than 4 teaspoonfuls (20 mL) in 24 hours
 children 2 to under 12 years of age take 1 teaspoonful (5 mL) every 12 hours; do not take more than 2 teaspoonfuls (10 mL) in 24 hours
 children under 2 years of age ask a doctor
 adults 65 years of age and older ask a doctor
 consumers with kidney disease ask a doctor

Other information

• each 5 mL (1 teaspoonful) contains: sodium 18 mg
• safety sealed: do not use if carton, unprinted foil inner seal, or neckband printed with “SEALED FOR YOUR PROTECTION” is opened, torn or missing.
•store between 20° to 25°C (68° to 77°F).
•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?

1-888-632-6900

PRINCIPAL DISPLAY PANEL

Compare to the active ingredient of Children’s Allegra® Allergy*see side panel
NDC 30142-527-94
Kroger®
NON-DROWSY
Ages 2 years and older 

Children’s
Allergy Relief 

Fexofenadine Hydrochloride Oral Suspension
30 mg/ 5mL
Antihistamine
12 HOURS  

Alcohol Free• Dye Free
Indoor & Outdoor Allergies 

12 Hour Relief of:

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

Use only with enclosed dosing cup. Wash and let air dry after each use. 

Berry Flavor 

4 fl. oz. (118 mL)

allergy relief
CHILDRENS ALLERGY RELIEF 
fexofenadine hydrochloride suspension
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:30142-527
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)  
Other Ingredients
Ingredient KindIngredient NameQuantity
Does not containALCOHOL (UNII: 3K9958V90M) 0   in 5 mL
Product Characteristics
Color    Score    
ShapeSize
FlavorBERRYImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:30142-527-941 in 1 CARTON07/01/201506/30/2018
1118 mL in 1 BOTTLE; Type 1: Convenience Kit of Co-Package
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
ANDAANDA20333007/01/201506/30/2018
Labeler - Kroger Company (006999528)
Registrant - Teva Pharmaceuticals USA, Inc. (001627975)
Establishment
NameAddressID/FEIBusiness Operations
G&W NC Laboratories, LLC079419931ANALYSIS(30142-527) , LABEL(30142-527) , MANUFACTURE(30142-527) , PACK(30142-527)

Revised: 12/2017
Document Id: aa7e25a3-b943-4d4c-a18c-e0b9ae975ec3
Set id: 9b007bd2-027a-43cb-b954-bb4e495cfad6
Version: 3
Effective Time: 20171214
 
Kroger Company