Hydroxyzine Hydrochloride Tablet, Film Coated
Product Images NDC 10702-012

11 FDA label images from Kvk-tech, Inc. · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 11 technical images submitted to the FDA as part of the official labeling for Hydroxyzine Hydrochloride (NDC 10702-012). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Kvk-tech, 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

01 Chemical Structure

01 Chemical Structure
Chemical structure diagram of Hydroxyzine Hydrochloride depicting the molecular formula C21H27ClN2O2•2HCl and molecular weight of 447.83.*
FDA Label Image
FDA Label Image

03 10mg 100s

03 10mg 100s
Hydroxyzine Hydrochloride Tablets USP 10 mg film-coated tablet label by KVK-Tech, Inc. The label states the active ingredient as Hydroxyzine HCl 10 mg per tablet, with a quantity of 100 tablets. It includes storage instructions at 20°C to 25°C, a barcode, and a note to keep medication out of children's reach.*
FDA Label Image

04 10mg 500s

04 10mg 500s
Hydroxyzine Hydrochloride Tablets USP 10 mg film-coated oral tablets packaging label. Shows strength as 10 mg, quantity of 500 tablets, and that the product is Rx only. Labeler is KVK-Tech, Inc. Includes storage instructions and a barcode.*
FDA Label Image

05 10mg 1000s

05 10mg 1000s
Label for Hydroxyzine Hydrochloride Tablets, USP 10 mg by KVK-Tech, Inc. The label indicates 1000 film-coated tablets, oral route, prescription only. Directions mention dispensing in a child-resistant container and storage between 20°C to 25°C. The tablet strength is prominently shown in orange with 10 mg dosage.*
FDA Label Image

06 25mg 100s

06 25mg 100s
Hydroxyzine Hydrochloride 25 mg film-coated tablet label from KVK-Tech, Inc. The label shows the product name, strength, quantity of 100 tablets per bottle, and NDC 10702-011-01. It includes storage instructions, dispensing guidelines, and manufacturer information.*
FDA Label Image

07 25mg 500s

07 25mg 500s
Label for Hydroxyzine Hydrochloride Tablets USP, 25 mg strength, film-coated tablets. The label states prescription use only (Rx Only) and packaging of 500 tablets. It includes dosage information, storage instructions, child-resistant packaging note, manufacturer as KVK-Tech, Inc., and a barcode.*
FDA Label Image

08 25mg 1000

08 25mg 1000
Label for Hydroxyzine Hydrochloride Tablets, USP 25 mg, film-coated oral tablets. The label indicates packaging of 1000 tablets and is manufactured by KVK-Tech, Inc. Dosage and storage instructions are partially visible, including storage at 20°C to 25°C with certain tolerated excursions and child-resistant container requirements.*
FDA Label Image

09 50mg 100s

09 50mg 100s
Label for Hydroxyzine Hydrochloride Tablets, USP 50 mg by KVK-Tech, Inc. The label states the dosage form as film-coated tablets, oral route, with a package count of 100 tablets. It includes storage instructions between 20°C to 25°C, dispensing and dosage guidance, and the manufacturer information in Newtown, PA, USA.*
FDA Label Image

10 50mg 500s

10 50mg 500s
Hydroxyzine Hydrochloride 50 mg film-coated tablets packaging label showing the product name, strength, and dosage form. The label indicates 500 tablets per container, Rx only, manufactured by KVK-Tech, Inc. Features include storage instructions, child-resistant closure notice, and barcode with the NDC 10702-012-50.*
FDA Label Image

11 50mg 1000s

11 50mg 1000s
Label panel for Hydroxyzine Hydrochloride Tablets, USP 50 mg by KVK-Tech, Inc. It specifies the active ingredient amount, package quantity of 1000 tablets, storage conditions, dispensing instructions, and a warning to keep out of reach of children. The panel includes the NDC number 10702-012-10 and manufacturer details.*

* 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.