Ice Blue Pain Alleviating Rub
Product Images NDC 82988-101

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Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Ice Blue Pain Alleviating Rub (NDC 82988-101). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Lemisol Corporation, 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

Principal Display Panel – 8 Oz Spray Label (Ice00 0000 01)

Principal Display Panel – 8 Oz Spray Label (Ice00 0000 01)
This is a Drug Facts label that provides information on the active ingredients, uses, warnings, and directions for a topical analgesic gel. The gel contains methyl salicylate, menthol, and camphor, and is designed to provide temporary relief from minor aches and pains associated with arthritis, backache, muscle strains, sprains, bruises, and cramps. The label includes warnings to use the product only externally and to avoid contact with eyes and mucous membranes, as well as directions for use by adults and children over 12 years of age. The label also warns against use on damaged or irritated skin, or with a heating pad. The Gel should not be applied to children under 2 years old. The text includes a disclaimer that it is distributed in the USA by LEMISOL Corporation in Miami, Florida.*
FDA Label Image

Principal Display Panel – 8 Oz Gel Label (Ice00 0000 02)

Principal Display Panel – 8 Oz Gel Label (Ice00 0000 02)
Teles Analgesic is a topical pain relief gel that contains menthol, methyl salicylate, and camphor as active ingredients. It provides temporary relief for minor aches and pains associated with arthritis, muscle strains, sprains, bruises, and cramps. However, it is only for external use, and users should not bandage or apply heating pads on the affected area. Teles Analgesic is not applicable to wounds or damaged skin, and caution is necessary to avoid contact with eyes and mucous membranes. If conditions worsen, irritation persists, or the symptoms remain for at least eight days, users are advised to see a doctor. Inactive ingredients include alcohol denatured, carbomer, cetrimonium chloride, cetyl alcohol, FD&C blue No.1, purified water, and triethanolamine. Users should apply a generous amount of the product to the affected area, massage until the gel dissolves completely, and repeat as needed. Children under 12 years of age should consult a doctor before use. For questions or inquiries, consumers can contact Emisol Corporation at 305-363-2696 or visit their website at www.mylemisol.com.*

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