Cetirizine Hydrochloride
Product Images NDC 67296-1085

Product Visual Gallery

This gallery contains 7 technical images submitted to the FDA as part of the official labeling for Cetirizine Hydrochloride (NDC 67296-1085). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Redpharm Drug, 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

30 Count (67296 1085)

Cetirizine Hydrochloride 10mg tablet label showing prescription-only status. The label includes the product NDC 67296-1085-3, lot number Y99038X1, and expiration date 06/21. It indicates 30 tablets per package, manufacturer as Unique Pharmaceutical Laboratories in Mumbai, India, and Redpharm Drug as the distributor in Eden Prairie, MN. Storage instructions specify controlled room temperature 20-25°C (68-77°F).*

FDA Label Image

Drugfact (Cetirizinelabel 10mg 100count Df)

Cetirizine Hydrochloride Tablets USP 10 mg, original prescription strength, with 100 tablets per bottle, labeled by RedPharm Drug. The label highlights use for allergy relief in adults and children aged 6 years and older, with dosage directions and warnings. The product is identified as an antihistamine for symptoms such as sneezing, runny nose, and itchy, watery eyes.*

FDA Label Image

Drugfact2 (Cetirizinelabel 10mg 100count Df2)

Drug Facts panel continuation for Cetirizine Hydrochloride by RedPharm Drug, presenting warnings about allergic reactions, advice to consult a doctor before use if liver or kidney disease is present, or when taking tranquilizers or sedatives. Includes precautions about drowsiness, alcohol use, pregnancy and breastfeeding, and keeping the product out of children's reach, with an emergency contact number provided.*

FDA Label Image

Label (Cetirizinelabel 10mg 100count)

Packaging label for Cetirizine Hydrochloride Tablets USP, 10 mg strength, indicating 100 tablets per package. The label includes dosage information for ages 6 years and older, lists active and inactive ingredients, manufacturer and distributor details, NDC 16571-402-10, lot and expiration number fields, and a barcode. Labeler is Rising Pharmaceuticals.*

FDA Label Image

Drugfact (Cetirizinelabel 10mg 500count Df)

Drug Facts panel showing directions for use and active ingredient information for Cetirizine Hydrochloride tablets USP 10 mg. The directions specify dosing instructions for adults, children, and special populations. The active ingredient is cetirizine HCl 10 mg per tablet with its purpose as an antihistamine. Uses and warnings related to symptoms of hay fever and upper respiratory allergies are included.*

FDA Label Image

Drugfact2 (Cetirizinelabel 10mg 500count Df2)

Drug Facts warning section from Cetirizine Hydrochloride by RedPharm Drug. It includes warnings not to use if allergic to ingredients or hydroxyzine, advice to ask a doctor before use if liver, kidney disease, or taking sedatives, cautions about drowsiness and avoiding alcohol, instructions to stop use if allergic reaction occurs, and warnings regarding pregnancy, breastfeeding, and keeping out of reach of children with Poison Control contact information.*

FDA Label Image

Label (Cetirizinelabel 10mg 500count)

Packaging label for Rising Cetirizine Hydrochloride Tablets USP, 10 mg strength. The label indicates the product is an original prescription strength, with 500 tablets in the package, intended for ages 6 years and older. It includes manufacturer and distributor information: manufactured by Unique Pharmaceutical Labs, Mumbai, India, and distributed by Rising Pharmaceuticals, Saddle Brook, NJ.*

* 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.