Blue Ice Analgesic Gel
Product Images NDC 61734-021

2 FDA label images from Delon Laboratories (1990) Ltd · 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 Blue Ice Analgesic (NDC 61734-021). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Delon Laboratories (1990) Ltd, 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

Delon Blue Ice Analgesic Gel 8oz (Delon Blue Ice Analgesic Gel 8oz)

Delon Blue Ice Analgesic Gel 8oz (Delon Blue Ice Analgesic Gel 8oz)
The packaging label for Blue Ice Analgesic Gel by Delon Laboratories features a predominantly blue background with white and red text. The product is a topical analgesic gel containing 2g of Menthol per 100g. The label indicates it provides temporary relief of minor aches and pains of muscles and joints. The net weight is 8 oz. Additional details include drug facts, warnings, directions, inactive ingredients, barcode, and a note that the product is not tested on animals.*
FDA Label Image

Penetro Blue Ice Analgesic Gel (Penetro Blue Ice Analgesic Gel 8 Oz (227 G))

Penetro Blue Ice Analgesic Gel (Penetro Blue Ice Analgesic Gel 8 Oz (227 G))
Label for Blue Ice Analgesic Gel by Delon Laboratories, containing 2 g/100g menthol as the active ingredient. The label states the product is a topical analgesic gel with a net weight of 8 oz (227 g). It includes Drug Facts, warnings, directions, and inactive ingredients, along with a barcode and distributor information. The design features a blue ice-themed background with red and white text accents.*

* 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.