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
ALLERGY RELIEF
- Manufacturer
- Bi-Mart | ScieGen Pharmaceuticals, INC.
- Effective date
- 2025-04-28
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 1
- Source
- full-release
- Hydrated at
- 2026-06-01 01:00:07
Label at a glance#
ProductALLERGY RELIEF
Active ingredientFEXOFENADINE HYDROCHLORIDE
Label structure10 sections
Dosage and administration
adults and children 12 years of age and over take one 180mg tablet with water once a day; do not take more than 1 tablet in 24 hours children under 12 years of age do not use adults 65 years of age and older ask a doctor consumers with kidney disease ask a doctor
Storage and handling
store between 20° and 25°C (68° and 77°F) protect from excessive moisture each tablet contains: sodium 8 mg this product meets the requirements of USP Dissolution Test 2
Contacts and useful links#
Label contents#
Full prescribing information#
Active ingredient (in each tablet)
Fexofenadine HCl 180 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.
OTC - PREGNANCY OR BREAST FEEDING SECTION
If pregnant or breast-feeding,
ask a health professional before use.
OTC - KEEP OUT OF REACH OF CHILDREN SECTION
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.
Directions
adults and children 12 years of age and over | take one 180mg tablet with water once a day; do not take more than 1 tablet in 24 hours |
children under 12 years of age | do not use |
adults 65 years of age and older | ask a doctor |
consumers with kidney disease | ask a doctor |
Other information
- store between 20° and 25°C (68° and 77°F)
- protect from excessive moisture
- each tablet contains: sodium 8 mg
- this product meets the requirements of USP Dissolution Test 2
Inactive ingredients
anhydrous lactose, colloidal silicon dioxide, corn starch, croscarmellose sodium, hypromellose, lactose monohydrate, polyethylene glycol, pregelatinized starch(maize), red iron oxide, stearic acid, titanium dioxide, yellow iron oxide.
Questions?
Call toll-free 1-844-912-4012
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
NDC 37835-601-09
COMPARE TO THE ACTIVE INGREDIENT IN ALLEGRA ®ALLERGY 24 HOUR TABLETS*
NON-DROWSY
ALLERGY RELIEF
FEXOFENADINE HYDROCHLORIDE 180 mg
24 HOUR ALLERGY
ORIGINAL PRESCRIPTION STRENGTH
RELIEF OF:
SNEEZING
RUNNY NOSE
ITCHY, WATER EYES
ITCHY NOSE OR THROAT
ANTIHISTAMINE
90 Tablets
*This product is not manufactured or distributed by the owner of the registered trademark Allegra ®Allergy 24 Hour Tablets.
Distributed by:
BI-MART
Eugene, OR 97402
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
NDC 37835-601-45
COMPARE TO THE ACTIVE INGREDIENT IN ALLEGRA ®ALLERGY 24 HOUR TABLETS*
NON-DROWSY
ALLERGY RELIEF
FEXOFENADINE HYDROCHLORIDE 180 mg
24 HOUR ALLERGY
ORIGINAL PRESCRIPTION STRENGTH
RELIEF OF:
SNEEZING
RUNNY NOSE
ITCHY, WATER EYES
ITCHY NOSE OR THROAT
ANTIHISTAMINE
45 Tablets
*This product is not manufactured or distributed by the owner of the registered trademark Allegra ®Allergy 24 Hour Tablets.
Distributed by:
BI-MART
Eugene, OR 97402
DailyMed RxNorm Mappings#
DailyMed Pharmacologic Classes#
| Class | Version | Type | Effective |
|---|---|---|---|
| FEXOFENADINE Pharmacologic Class Indexing | 3 | Indexing - Pharmacologic Class | 20180813 |
DailyMed Product Concepts#
| Product concept | Relation | Version | Effective |
|---|---|---|---|
| b893258d-0942-3d8a-3411-056ea0788ff5 | Product name | 1 | 20140508 |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 37835-601-09 | ALLERGY RELIEF | 90 in 1 BOTTLE | TABLET, FILM COATED | 90 | 1 | |
| 37835-601-45 | ALLERGY RELIEF | 45 in 1 BOTTLE | TABLET, FILM COATED | 45 | 1 |
DailyMed Dashboard NDC Coverage#
Products#
Every source-derived product name is available through these pages.
- ALLERGY RELIEF
- fexofenadine hcl
- ANHYDROUS LACTOSE
- SILICON DIOXIDE
- STARCH, CORN
- CROSCARMELLOSE SODIUM
- LACTOSE MONOHYDRATE
- STEARIC ACID
- HYPROMELLOSE, UNSPECIFIED
- POLYETHYLENE GLYCOL, UNSPECIFIED
- FERRIC OXIDE RED
- TITANIUM DIOXIDE
- FERRIC OXIDE YELLOW
- FEXOFENADINE HYDROCHLORIDE
- FEXOFENADINE
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 37835-601 | 37835-601-45, 37835-601-09 |
Ingredients#
Every source-derived ingredient row is available through these pages.
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 |
|---|---|---|---|---|---|---|
| 33d56c1c-22da-e750-e063-6294a90ae6d0 | ea8d8e12-4781-4501-a887-e732295d33bf | 2025-04-28 | Warnings | 33d56c1c-22da-e750-e063-6294a90ae6d0 ea8d8e12-4781-4501-a887-e732295d33bf |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.