Search by Drug Name or NDC
NDC 37808-0425-53 Allergy Relief 60 mg/1 Details
Allergy Relief 60 mg/1
Allergy Relief is a ORAL TABLET, FILM COATED in the HUMAN OTC DRUG category. It is labeled and distributed by H E B. The primary component is FEXOFENADINE HYDROCHLORIDE.
MedlinePlus Drug Summary
Fexofenadine is used to relieve the allergy symptoms of seasonal allergic rhinitis (''hay fever''), including runny nose; sneezing; red, itchy, or watery eyes; or itching of the nose, throat, or roof of the mouth in adults and children 2 years of age and older. It is also used to relieve symptoms of urticaria (hives; red, itchy raised areas of the skin), including itching and rash in adults and children 6 months of age and older. Fexofenadine is in a class of medications called antihistamines. It works by blocking the effects of histamine, a substance in the body that causes allergy symptoms.
Related Packages: 37808-0425-53Last Updated: 11/30/2022
MedLinePlus Full Drug Details: Fexofenadine
Product Information
NDC | 37808-0425 |
---|---|
Product ID | 37808-425_570179ef-c32d-4afa-90cb-24966184041e |
Associated GPIs | |
GCN Sequence Number | n/a |
GCN Sequence Number Description | n/a |
HIC3 | n/a |
HIC3 Description | n/a |
GCN | n/a |
HICL Sequence Number | n/a |
HICL Sequence Number Description | n/a |
Brand/Generic | n/a |
Proprietary Name | Allergy Relief |
Proprietary Name Suffix | n/a |
Non-Proprietary Name | Fexofenadine HCl |
Product Type | HUMAN OTC DRUG |
Dosage Form | TABLET, FILM COATED |
Route | ORAL |
Active Ingredient Strength | 60 |
Active Ingredient Units | mg/1 |
Substance Name | FEXOFENADINE HYDROCHLORIDE |
Labeler Name | H E B |
Pharmaceutical Class | Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC] |
DEA Schedule | n/a |
Marketing Category | ANDA |
Application Number | ANDA076447 |
Listing Certified Through | 2024-12-31 |
Package
Package Images

NDC 37808-0425-53 (37808042553)
NDC Package Code | 37808-425-53 |
---|---|
Billing NDC | 37808042553 |
Package | 12 BLISTER PACK in 1 CARTON (37808-425-53) / 1 TABLET, FILM COATED in 1 BLISTER PACK |
Marketing Start Date | 2011-08-24 |
NDC Exclude Flag | N |
Pricing Information | N/A |
Standard Product Labeling (SPL)/Prescribing Information SPL 55af2c65-6db9-4abc-94e6-df88b99dfc60 Details
Uses
Warnings
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)
Directions
Other information
Inactive ingredients
Package/Label Principal Display Panel
INGREDIENTS AND APPEARANCE
ALLERGY RELIEF
fexofenadine hcl tablet, film coated |
||||||||||||||||||||||||||||
|
||||||||||||||||||||||||||||
|
||||||||||||||||||||||||||||
|
||||||||||||||||||||||||||||
|
||||||||||||||||||||||||||||
|
||||||||||||||||||||||||||||
|
Labeler - H E B (007924756) |