Hydroxyzine Hydrochloride Tablet, Film Coated
Product Images NDC 62135-545

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 7 technical images submitted to the FDA as part of the official labeling for Hydroxyzine Hydrochloride (NDC 62135-545). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Chartwell Rx, Llc, 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

"image Description" (Hydroxyzine Hydrochloride 10mg 120 Label)

"image Description" (Hydroxyzine Hydrochloride 10mg 120 Label)
Label for Hydroxyzine Hydrochloride 10 mg tablets, USP, film-coated, oral use. The label indicates a package of 120 tablets labeled 'Rx Only' by Chartwell RX, LLC. Instructions include storage conditions and cautions about keeping the medication out of reach of children. The label features the NDC 62135-545-12 and a barcode.*
FDA Label Image

"image Description" (Hydroxyzine Hydrochloride 10mg 500 Label)

"image Description" (Hydroxyzine Hydrochloride 10mg 500 Label)
Label for Hydroxyzine Hydrochloride Tablets, USP 10 mg oral dose, containing 500 tablets. The label includes the NDC code 62135-545-05 and states the product is for prescription use only. It is manufactured for Chartwell RX, LLC in Congers, NY, with storage instructions and a barcode present. The label also includes a statement about child-resistant packaging and medication safety.*
FDA Label Image

"image Description" (Hydroxyzine Hydrochloride 25mg 120 Label)

"image Description" (Hydroxyzine Hydrochloride 25mg 120 Label)
Hydroxyzine Hydrochloride 25 mg film-coated tablets label, USP, oral administration. The label states it is prescription only and contains 120 tablets. Manufactured by Chartwell RX, LLC, the packaging provides storage instructions and cautions about contamination and child safety. A barcode and NDC number 62135-546-12 are visible.*
FDA Label Image

"image Description" (Hydroxyzine Hydrochloride 25mg 500 Label)

"image Description" (Hydroxyzine Hydrochloride 25mg 500 Label)
Label for Hydroxyzine Hydrochloride Tablets, USP 25 mg by Chartwell RX, LLC. The label indicates a package size of 500 film-coated tablets, with storage and handling instructions. The label displays the NDC number 62135-546-05 and a barcode.*
FDA Label Image

"image Description" (Hydroxyzine Hydrochloride 50mg 120 Label)

"image Description" (Hydroxyzine Hydrochloride 50mg 120 Label)
Label for Hydroxyzine Hydrochloride 50 mg film-coated tablets by Chartwell RX, LLC. The label states the product contains 120 tablets, is for prescription use only, and includes storage and dispensing instructions. The NDC code is 62135-547-12.*
FDA Label Image

"image Description" (Hydroxyzine Hydrochloride 50mg 500 Label)

"image Description" (Hydroxyzine Hydrochloride 50mg 500 Label)
The label for Hydroxyzine Hydrochloride 50 mg tablets, USP, identifies the product as prescription only with a quantity of 500 tablets. The label features bold black and purple text with the strength prominently displayed. The labeler is Chartwell Rx, LLC, located in Congers, NY. Storage and dispensing instructions are included in small print alongside a barcode.*
FDA Label Image

"image Description" (Hydroxyzine Hydrochloride Structure)

"image Description" (Hydroxyzine Hydrochloride Structure)
Chemical structure diagram of Hydroxyzine Hydrochloride, showing the molecular arrangement including aromatic rings, nitrogen atoms, chlorine, and hydroxyl groups with the 2HCl indicated as part of the composition.*

* 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.