Fexofenadine Hydrochloride
Product Images NDC 62756-543

Product Visual Gallery

This gallery contains 14 technical images submitted to the FDA as part of the official labeling for Fexofenadine Hydrochloride (NDC 62756-543). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Sun Pharmaceutical Industries, Inc., these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

FDA Label Image

180mg-allergy-1 (180mg Allergy 1)

Label for Fexofenadine Hydrochloride Tablets USP 180 mg by Sun Pharmaceutical Industries, Inc. The label states it is an allergy medication for relief of sneezing, runny nose, itchy watery eyes, and itchy nose or throat. The package contains 100 tablets, each 180 mg, intended as a non-drowsy, 24-hour antihistamine. Includes manufacturer and distributor information along with NDC 62756-545-88.*

FDA Label Image

180mg-allergy-2 (180mg Allergy 2)

Drug Facts panel for Fexofenadine Hydrochloride 180 mg tablets by Sun Pharmaceutical Industries, Inc. It lists active ingredient, purpose, uses, warnings, directions for adults and children, and other information including storage instructions and inactive ingredients.*

FDA Label Image

180mg-allergy-sb (180mg Allergy Sb)

Drug Facts panels for Fexofenadine Hydrochloride Tablets, USP 180 mg by Sun Pharmaceutical Industries, Inc. The panels detail active ingredient, purpose, uses, warnings, directions for adults and children, inactive ingredients, and additional safety information including storage instructions.*

FDA Label Image

30mg-allergy-2 (30mg Allergy 2)

Drug Facts panel for Fexofenadine Hydrochloride showing the active ingredient as Fexofenadine HCl, USP 30 mg per tablet. It lists the purpose as an antihistamine and states its use for temporarily relieving symptoms due to hay fever or other upper respiratory allergies.*

FDA Label Image

30mg-allergy-3 (30mg Allergy 3)

A two-part continuous Drug Facts panel for FEXOFENADINE HYDROCHLORIDE by Sun Pharmaceutical Industries, Inc. The first panel lists symptoms treated such as runny nose, sneezing, itchy, watery eyes, and itching of the nose or throat, along with a warning against use if allergic. The second panel advises consulting a doctor before use if kidney disease is present and cautions against exceeding directed dose or taking with certain antacids or fruit juices.*

FDA Label Image

30mg-allergy-4 (30mg Allergy 4)

Two Drug Facts panels continuing safety and directions information. The first panel advises stopping use if allergic reaction occurs, consulting a doctor if pregnant or breast-feeding, and keeping out of reach of children with poison control instructions in case of overdose. The second panel provides dosing directions for adults and children 12 years and older, and for children 6 to under 12 years, specifying tablet amounts and timing.*

FDA Label Image

30mg-allergy-5 (30mg Allergy 5)

Continuation of the Drug Facts panel for FEXOFENADINE HYDROCHLORIDE including usage warnings for children under 6 years, adults 65 and older, and consumers with kidney disease. Additional information covers safety sealing, storage conditions, and a list of inactive ingredients: crospovidone, hypromellose, and iron oxide red.*

FDA Label Image

30mg-allergy-6 (30mg Allergy 6)

Continuation of the Drug Facts panel for Fexofenadine Hydrochloride, listing inactive ingredients including iron oxide yellow, magnesium stearate, microcrystalline cellulose, polyethylene glycol, pregelatinized starch, and titanium dioxide. Includes a customer service contact phone number for questions.*

FDA Label Image

30mg-allergy-7 (30mg Allergy 7)

Label for Children's Fexofenadine Hydrochloride Tablets USP 30 mg by Sun Pharmaceutical Industries, Inc. The label states the product as an antihistamine for indoor and outdoor allergies, with 100 tablets of 30 mg strength. It includes safety seal instructions, non-drowsy warning, age indication (6 years and older), and relieves symptoms such as sneezing, runny nose, itchy watery eyes, and itchy nose or throat. Distributed by Caraco Pharmaceutical Laboratories.*

FDA Label Image

30mg-allergy-sb (30mg Allergy Sb)

Drug Facts panels for Fexofenadine Hydrochloride Tablets, USP 30 mg by Sun Pharmaceutical Industries, Inc. including active ingredient, purpose as an antihistamine, uses for relief of allergy symptoms, warnings, directions for various age groups, inactive ingredients, questions contact, and additional safety and storage information.*

FDA Label Image

60mg-allergy-1 (60mg Allergy 1)

The label for Fexofenadine Hydrochloride Tablets, USP, 60 mg, an antihistamine for indoor and outdoor allergies. It indicates non-drowsy relief for symptoms such as sneezing, runny nose, itchy watery eyes, and itchy nose or throat. The package contains 100 tablets of 60 mg each. The label also includes manufacturer information for Sun Pharmaceutical Industries, Inc., and distributor details for Caraco Pharmaceutical Laboratories.*

FDA Label Image

60mg-allergy-2 (60mg Allergy 2)

Drug Facts text panel for Fexofenadine Hydrochloride 60 mg provides information on active ingredient, uses as an antihistamine to temporarily relieve allergy symptoms, warnings about allergy to the product and kidney disease, dosage directions, and advice on consulting a doctor for children, pregnant or breast-feeding individuals.*

FDA Label Image

60mg-allergy-3 (60mg Allergy 3)

The image shows a continued Drug Facts panel for Fexofenadine Hydrochloride. It includes directions for dosage, warnings for age and kidney disease, storage instructions, a list of inactive ingredients such as yellow and red iron oxides, magnesium stearate, and others, and a contact number for questions. The text is organized in tables and columns.*

FDA Label Image

60mg-allergy-sb (60mg Allergy Sb)

Drug Facts panel for Fexofenadine Hydrochloride Tablets, USP 60 mg by Sun Pharmaceutical Industries, listing active ingredient, uses for allergy symptom relief, warnings, directions for various age groups, inactive ingredients, and additional consumer safety information.*

* About these descriptions: Image descriptions on this page are generated by automated AI analysis of the product label images from the manufacturer's FDA label submission (SPL). They are provided for reference only and may contain errors or omissions. Always rely on the printed label itself and the official FDA labeling, and consult a pharmacist or healthcare professional with any questions about this product.