Indications and 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
Children Allergy
- Manufacturer
- H E B
- Effective date
- 2024-01-03
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 2
- Source
- legacy-cache
- Hydrated at
- 2026-08-01 21:16:10
Label at a glance#
ProductChildren Allergy
Active ingredientFEXOFENADINE HYDROCHLORIDE
Label structure10 sections
Storage and handling
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.
Contacts and useful links#
Label contents#
Full prescribing information#
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 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 |
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
Children's Allergy
Fexofenadine HCl Oral Suspension
30 mg/ 5 mL
Antihistamine
Indoor/Outdoor allergy relief
- Sneezing
- Runny nose
- Itchy, watery eyes
- Itchy nose or throat
12 Hour Relief
Ages 2 years and older
Non-drowsy
Dye-Free
Alcohol-free
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.
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 .
MADE WITH PRIDE AND CARE FOR H-E-B®, SAN ANTONIO, TX 78204
Product Label
Products#
Every source-derived product name is available through these pages.
- Children Allergy
- Fexofenadine HCl
- FEXOFENADINE HYDROCHLORIDE
- FEXOFENADINE
- BUTYLPARABEN
- EDETATE DISODIUM
- POLOXAMER 407
- PROPYLENE GLYCOL
- PROPYLPARABEN
- WATER
- SODIUM PHOSPHATE, DIBASIC, ANHYDROUS
- SODIUM PHOSPHATE, MONOBASIC, ANHYDROUS
- SUCROSE
- TITANIUM DIOXIDE
- XANTHAN GUM
- XYLITOL
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 37808-226 | 37808-226-04 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| FEXOFENADINE HYDROCHLORIDE | 2S068B75ZU | ACTIB |
| BUTYLPARABEN | 3QPI1U3FV8 | IACT |
| EDETATE DISODIUM | 7FLD91C86K | IACT |
| POLOXAMER 407 | TUF2IVW3M2 | IACT |
| PROPYLENE GLYCOL | 6DC9Q167V3 | IACT |
| PROPYLPARABEN | Z8IX2SC1OH | IACT |
| WATER | 059QF0KO0R | IACT |
| SODIUM PHOSPHATE, DIBASIC, ANHYDROUS | 22ADO53M6F | IACT |
| SODIUM PHOSPHATE, MONOBASIC, ANHYDROUS | KH7I04HPUU | IACT |
| SUCROSE | C151H8M554 | IACT |
| TITANIUM DIOXIDE | 15FIX9V2JP | IACT |
| XANTHAN GUM | TTV12P4NEE | IACT |
| XYLITOL | VCQ006KQ1E | IACT |
Source Document#
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| 9a85857a-84c7-48d3-aa2a-dc27e8c8f5f3 | dd70a634-beca-4282-8f56-ad0957906609 | 2024-01-03 | Warnings | 9a85857a-84c7-48d3-aa2a-dc27e8c8f5f3 dd70a634-beca-4282-8f56-ad0957906609 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.