Neuroflex Topical Pain Relieving Liquid Solution
Product Images NDC 69876-1740

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This gallery contains 1 technical images submitted to the FDA as part of the official labeling for Neuroflex Topical Pain Relieving Liquid (NDC 69876-1740). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Almark Products 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.

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FDA Label Image

Label (Label)

Label (Label)
This is a drug facts label for a topical pain relieving liquid containing active ingredients camphor and menthol. The product is used for temporary relief of minor muscle and joint aches and pains associated with conditions such as arthritis, backaches, soreness, strains, sprains, and bruises. The product should only be used externally and should not be applied to wounds or damaged skin, mucous membranes, or eyes. The label indicates that the product is non-staining and greaseless, and includes contact information for the manufacturer in case of questions or concerns. Inactive ingredients listed include Eucalyptus Globulus Lead (Eucaluptus) O, Melaleuca, ERiNoAGRE: R Aternifolia (australian Tea Tree) Leat Oil, Pinus Sylvestis {Pine) O, olysorbate-20, and SD-Alcohol 40.*

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.