Bioactil
Product Images NDC 69492-013

Product Visual Gallery

This gallery contains 13 technical images submitted to the FDA as part of the official labeling for Bioactil (NDC 69492-013). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Polimeros Y Servicios S.a., 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 (Activeingredient)

This is a drug facts label that lists the active ingredient as "Menthol" at a concentration of 0.3%. The purpose of this ingredient is as a topical analgesic.*

FDA Label Image

Image Description (Bioactil 6 Frente)

FDA Label Image

Image Description (Bioactil Box)

This is a drug facts label belonging to a gel used for pain relief with the brand name BIOACTIL. The product is said to help with backaches, hard-working and hard-playing muscles and joints, sprains and strains. It contains active ingredients (unnamed) and has inactive ingredients. The net weight of the product is 2.46 oz (70.6 g). A phone number is provided for questions or comments about the product.*

FDA Label Image

Image Description (Bioactilbox)

This is a drug intended to provide topical analgesic relief to sore muscles and joints associated with backaches, arthritis, sprains, and bruises. It contains 3% Menthol and is not recommended for children under two years old. The drug should be applied to the affected area, not more than 3-4 times daily. Inactive ingredients include carbomer, cetostearyl alcohol, and purified demineralized water, among others. It is manufactured by Polimeros y Servicios, S.A. in Costa Rica and distributed in the US by Med-Actil, LLC.*

FDA Label Image

Image Description (Bioactilfrente)

FDA Label Image

Image Description (Directions)

This text provides directions for the use of an unspecified gel. Adults and children over 12 years old can apply the gel up to 3-4 times a day and should gently massage the affected area until the gel disappears. However, children under the age of 12 should not use the gel and should consult a doctor.*

FDA Label Image

Image Description (Inactiveingredients)

This text describes the inactive ingredients present in a product or medication. The product contains carbomer, cetostearyl alcohol, cetostearyl ether, diazolidinyl urea, glycerin, methyl paraben, orthosilicic acid, phosphate buffer, propyl paraben, purified de-mineralized water, and salicylic acid. These ingredients are not the active ingredients that are responsible for the intended effects of the product but are included for other purposes such as formulation, stabilization, preservation, and improvement of sensorial properties.*

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Image Description (Keepoutofreachofchildrenbioactil)

This is a warning label advising to keep a product out of reach of children to avoid accidental poisoning. In case of ingestion, the text advises seeking medical help or contacting a Poison Control center immediately.*

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Image Description (Otherinformation)

This text provides instructions on how to store a product at a controlled room temperature between 15-30°C (59-86°F). It also indicates that the product has a lot number and expiration date that can be found on the box or crimp of the tube.*

FDA Label Image

Image Description (Purpose)

This is a Drug Facts label that provides information about the active ingredient Menthol and its purpose as a topical analgesic.*

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Image Description (Questionsorcomments)

This is a contact information for Med-Act company. They provide a phone number and a website for customers to reach them with any questions or comments. Med-Act manufactures products and is distributed by Med-Act, LLC. The company is located in Galveston, TX.*

FDA Label Image

Image Description (Uses)

This is a product that provides soothing relief to minor aches and pains of sore muscles and joints associated with arthritis, backache, strains, sprains, and bruises.*

FDA Label Image

Image Description (Warning)

This text appears to be a warning for external use of a product. It advises to use the product only as directed and to avoid contact with eyes or mucous membranes. If there is excessive irritation of the skin, the use of the product should be discontinued. Additionally, it warns against bandaging the area where the product is applied.*

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