DailyMed - DYE FREE WAL FEX CHILDRENS ALLERGY- fexofenadine hcl suspension

NDC Code(s): 0363-9230-04, 0363-9230-08
Packager: Walgreens

Category: HUMAN OTC DRUG LABEL
DEA Schedule: None
Marketing Status: Abbreviated New Drug Application

Drug Label Information

Updated June 23, 2022

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Active ingredient (in each 5 mL)
Fexofenadine HCL, USP 30 mg

Fexofenadine HCL, USP 30 mg
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Purpose
Antihistamine

Antihistamine
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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
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
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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 ...
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.

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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 ...

Other information
each 5 mL contains: sodium 18 mg - store between 20º to 25ºC (68º and 77ºF) before using any medication, read all label directions. Keep carton, it contains important information.
- each 5 mL contains: sodium 18 mg
- store between 20º to 25ºC (68º and 77ºF)
- before using any medication, read all label directions. Keep carton, it contains important information.
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Inactive ingredients
artificial raspberry flavor, butylparaben, edetate disodium, poloxamer 407, propylene glycol, propylparaben, purified water, sodium phosphate dibasic, sodium phosphate monobasic, sucrose, titanium ...

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
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Questions or comments?
Call 1-877-753-3935 Monday-Friday 9AM-5PM EST

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

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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 /PER 5 mL / ANTIHISTAMINE - DYE ...
*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 /PER 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)

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.

KEEP OUTER CARTON FOR COMPLETE WARNINGS AND PRODUCT INFORMATION

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

DISTRIBUTED BY: WALGREEN CO.

200 WILMOT RD., DEERFIELD, IL 60015

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Product Label
WALGREENS Children's Allergy Relief Berry Flavor

WALGREENS Children's Allergy Relief Berry Flavor

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INGREDIENTS AND APPEARANCE

Product Information

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Published Date (What is this?)	Version	Files
Jun 27, 2022	7 (current)	download
Apr 4, 2022	6	download
Mar 11, 2022	5	download
Aug 3, 2021	4	download
Jun 1, 2020	3	download

	RxCUI	RxNorm NAME	RxTTY
1	997491	fexofenadine HCl 30 MG in 5 mL Oral Suspension	PSN
2	997491	fexofenadine hydrochloride 6 MG/ML Oral Suspension	SCD
3	997491	fexofenadine HCl 30 MG per 5 ML Oral Suspension	SY
4	1670344	Wal-Fex 30 MG in 5 mL Oral Suspension	PSN
5	1670344	fexofenadine hydrochloride 6 MG/ML Oral Suspension [Wal-Fex]	SBD
6	1670344	Wal-Fex 30 MG per 5 ML Oral Suspension	SY
7	1670344	Wal-Fex 6 MG/ML Oral Suspension	SY

Label: DYE FREE WAL FEX CHILDRENS ALLERGY- fexofenadine hcl suspension

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Drug Label Info

Safety

Related Resources

More Info For This Drug

Drug Label Information

Do not use

Ask a doctor before use if you have

When using this product

Stop use and ask a doctor if

If pregnant or breast-feeding,

Keep out of reach of children.

Find additional resources

Safety

Related Resources

More Info on this Drug

adults and children 12 years of age and over	take 10 mL every 12 hours; do not take more than 20 mL in 24 hours
children 2 to under 12 years of age	take 5 mL every 12 hours; do not take more than 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

	NDC
1	0363-9230-04
2	0363-9230-08

Label: DYE FREE WAL FEX CHILDRENS ALLERGY- fexofenadine hcl suspension

View Package Photos

Drug Label Info

Safety

Related Resources

More Info For This Drug

Drug Label Information

Do not use

Ask a doctor before use if you have

When using this product

Stop use and ask a doctor if

If pregnant or breast-feeding,

Keep out of reach of children.

Find additional resources

Safety

Related Resources

More Info on this Drug

DYE FREE WAL FEX CHILDRENS ALLERGY- fexofenadine hcl suspension

Number of versions: 5

DYE FREE WAL FEX CHILDRENS ALLERGY- fexofenadine hcl suspension

DYE FREE WAL FEX CHILDRENS ALLERGY- fexofenadine hcl suspension

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DYE FREE WAL FEX CHILDRENS ALLERGY- fexofenadine hcl suspension

If this SPL contains inactivated NDCs listed by the FDA initiated compliance action, they will be specified as such.