Fexofenadine Hcl Tablet, Film Coated
Product Images NDC 50228-201

Product Visual Gallery

This gallery contains 8 technical images submitted to the FDA as part of the official labeling for Fexofenadine Hcl (NDC 50228-201). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Sciegen Pharmaceuticals, 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

Sciegen Pharmaceuticals, Inc. (Fexofenadine Allergy 09)

Label for Fexofenadine Hydrochloride Tablets, USP 60 mg film-coated tablets by ScieGen Pharmaceuticals, Inc. The label states the product is a non-drowsy antihistamine for allergy relief, with 30 tablets per container. It highlights 12-hour relief for indoor and outdoor allergy symptoms such as sneezing, runny nose, itchy watery eyes, and itchy nose or throat.*

FDA Label Image

Sciegen Pharmaceuticals, Inc. (Fexofenadine Allergy 10)

Drug Facts panel for fexofenadine hydrochloride 60 mg film-coated tablets providing information on active ingredient, purpose as an antihistamine, uses for relief of allergy symptoms, warnings, directions, and other product information including inactive ingredients and manufacturer details from ScieGen Pharmaceuticals, Inc.*

FDA Label Image

Sciegen Pharmaceuticals, Inc. (Fexofenadine Allergy 11)

Label for fexofenadine hydrochloride 180 mg film-coated tablets by ScieGen Pharmaceuticals, Inc. The label highlights allergy relief for indoor and outdoor allergies with 24-hour effectiveness. It includes a Drug Facts panel listing active ingredient, uses, warnings, directions, and inactive ingredients. The packaging is for a 30-tablet count with original prescription strength noted as non-drowsy.*

FDA Label Image

Sciegen Pharmaceuticals, Inc. (Fexofenadine Allergy 12)

Label for fexofenadine hydrochloride tablets, USP 180 mg, an antihistamine by ScieGen Pharmaceuticals, Inc. The label indicates the product is non-drowsy and used for allergy relief with 1,000 tablets per container. The Drug Facts panel provides active ingredient strength, uses, warnings, directions, storage instructions, inactive ingredients, and manufacturer information in Hauppauge, NY.*

FDA Label Image

Sciegen Pharmaceuticals, Inc. (Fexofenadine Hives 03)

Label for fexofenadine hydrochloride tablets USP, 60 mg antihistamine strength, with 30 tablets per package. The front prominently lists relief for hives itching lasting 12 hours. The labeler is ScieGen Pharmaceuticals, Inc. The back panel includes detailed Drug Facts covering active ingredient, purpose, uses, warnings, directions, storage, inactive ingredients, and contact information.*

FDA Label Image

Sciegen Pharmaceuticals, Inc. (Fexofenadine Hives 04)

Label for Fexofenadine Hydrochloride Tablets, USP 60 mg, an oral film-coated tablet for antihistamine use by ScieGen Pharmaceuticals, Inc. The label states the product is non-drowsy and intended for relief of itching due to hives with 12-hour duration. It shows a package size of 1,000 tablets, each containing 60 mg of the active ingredient.*

FDA Label Image

Sciegen Pharmaceuticals, Inc. (Fexofenadine Hives 05)

Drug Facts label for fexofenadine hydrochloride 180 mg film-coated tablets by ScieGen Pharmaceuticals, Inc. Includes active ingredient, purpose, uses, warnings, directions, other information, and inactive ingredients. The label provides details on usage for hives and itching relief, allergy warnings, storage instructions, and dosage recommendations for different age groups.*

FDA Label Image

Sciegen Pharmaceuticals, Inc. (Fexofenadine Hives 06)

The label is for fexofenadine hydrochloride tablets, USP, original prescription strength 180 mg, non-drowsy antihistamine. It is indicated for relief of itching due to hives for 24 hours. The package contains 1,000 film-coated tablets, each 180 mg, manufactured by ScieGen Pharmaceuticals, Inc. Directions and drug facts are printed on the label, including warnings, uses, and inactive ingredients.*

* 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.