Tecnu Calagel
Product Images NDC 51879-802

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Tecnu Calagel (NDC 51879-802). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Tec Laboratories 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

Calagel (2019 Calagel 6oz Vert Label Alternate R3)

Tecnu Calagel 20 mg/g gel label showing the product name, Diphenhydramine Hydrochloride as the active ingredient, and its classification as a topical analgesic. The label highlights its use for anti-itch relief from poison ivy, oak, sumac, insect bites, minor burns, sunburns, scrapes, and minor cuts. It includes the net weight of 6 oz (170 g) and the labeler Tec Laboratories Inc. The label also features a detailed Drug Facts panel and barcode.*

FDA Label Image

Calagel Pop (2019 Calagel 6oz Vert Pop Ol(1) (002))

Tecnu Calagel Anti-Itch Gel containing Diphenhydramine Hydrochloride 20 mg/g in a topical gel form. The carton shows the product as a maximum strength topical analgesic intended to relieve itching and pain caused by bites, sunburns, and minor skin irritations. The labeler is Tec Laboratories Inc. The packaging includes usage instructions and comparison information between pink and clear formulations.*

FDA Label Image

2019 Calagel Dispenser Vert R4a

Tecnu Calagel Anti-Itch Gel packaging label for topical analgesic gel containing Diphenhydramine Hydrochloride 20 mg/g. The label shows a green and white design with the Tecnu logo and highlights the product as a maximum strength anti-itch gel. It includes images of the product range, drug facts, warnings, and usage directions. The labeler is Tec Laboratories Inc.*

* 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.