Levocetirizine Dihydrochloride Tablet, Film Coated
Product Images NDC 69230-321

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Levocetirizine Dihydrochloride (NDC 69230-321). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Camber Consumer Care 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

Bottle Label (Bottle Label)

Bottle Label (Bottle Label)
This is a description of an allergy relief medication containing Levocetirizine dihydrochloride USP 5 mg as an active ingredient. It temporarily relieves symptoms due to hay fever or other respiratory allergies such as runny nose, sneezing, itchy nose or throat and itchy, watery eyes. The medicine must not be used by people who have kidney diseases or have had any allergic reaction to this product or any antihistamine containing cetirizine. Individuals who have difficulty emptying their bladder or have ever experienced drowsiness after using antihistamines should consult their doctor before use. This medicine is not recommended for pregnant or breastfeeding women. Adults over 65 years of age should seek their doctor's advice. The medication comes in tablet form, and the recommended dose is one tablet once a day in the evening, and one-half tablet for children aged 6-11, also taken daily in the evening. The product should be kept between 20° and 25°C (68° and 77°F) and must not be used if the printed foil inner seal on the bottle is torn or missing. For more information or comments, call 1-888-588-1418.*
FDA Label Image

Carton (Carton)

Carton (Carton)
This is a drug information sheet that provides details, warnings, uses, and directions on the use of Camber NDC, a medication that temporarily relieves respiratory allergy symptoms caused by hay fever such as runny nose, itchy and watery eyes, throat, and sneezing. It also contains possible drowsiness as one of its side-effects, and precautions should be taken when driving or operating machinery. The inactive ingredients are identified as colloidal silicon dioxide, hypromellose, lactose monohydrate, magnesium stearate, microcrystalline cellulose, polyethylene glycol, polysorbate 80, and titanium dioxide.*

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.