Product Images Cetirizine Hydrochloride

This is a description of Cetirizine Hydrochloride Tablets, USP with a strength of 10mg, containing 100 tablets for individuals of age 6 years and above. The NDC number for this medicine is 16571-402-10, and it is manufactured by Unique Pharmaceutical Labs, a division of J.8. Chemicals & Pharmaceuticals Ltd., owned by Rising Pharma Holdings, Inc. The production date of this batch is July 2020.*

This is a drug information label for Cetirizine Hydrochloride, an antihistamine tablet used for temporary relief of symptoms caused by hay fever or upper respiratory allergies. The drug is available in the form of 100 tablets per bottle, and the recommended dosage for adults and children above 6 years old is one 10 mg tablet once daily. For those aged 65 and over or with certain medical conditions, it is recommended to consult a physician before using the product. The drug is not recommended for children under 6 years old. This provides drug facts, including the active ingredient, Cetirizine HCI USP 10 mg.*

This is a drug label or package insert containing warnings and instructions for use. It advises not to use the product if the user has an allergy to it or its components, to avoid alcohol and certain drugs that could increase drowsiness, and to be careful when driving or operating a machine. It also suggests consulting a doctor before use if the user has liver or kidney disease, and to seek medical help immediately if an allergic reaction occurs. It warns about keeping the product out of reach of children and what to do in case of an overdose.*

This is a drug label for Cetirizine Hydrochloride Tablets USP. It contains important drug facts, dosage directions, and warns not to take more than one 10 mg tablet per day for adults and children over six years of age or a 5mg product may be appropriate for smaller sizes. It's used for temporary relief of symptoms due to hay fever or other upper respiratory allergies such as a runny nose, sneezing, watery or itchy eyes. This product is not recommended for children under six years old and those over 65 years old should consult a doctor before use. The label also states not to use if the foil inner seal is broken or missing.*

This is a section of a medication's drug facts that contains warnings and precautions. It advises against using alcohol and other sedative-containing products while using this medication, as they may increase drowsiness. It also mentions the possibility of an allergic reaction and advises seeking medical help if such a reaction occurs. It then gives recommendations for people with specific health conditions and advises against using this medication during pregnancy or while breastfeeding without consulting a doctor. Finally, it reminds users to keep the medication out of reach of children and provides emergency contact information.*