Neotica
Product Images NDC 72398-000

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Neotica (NDC 72398-000). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Lost Tree Health, Llc, 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

Label (Label)

Label (Label)
This is a drug facts sheet for a topical pain relief product. The active ingredients include Menthol 5.64% and Ve Sy 125~ e g, and it is used to relieve minor aches and pains of muscles and joints. The product is for external use only and should not be applied to wounds or damaged skin. The directions specify applying it to affected areas not more than 3 to 4 times daily, while keeping it away from the eyes and mucous membranes. If severe skin irritation occurs, one should seek medical attention.*
FDA Label Image

Label2 (Label2)

Label2 (Label2)
This document contains information about a drug product, which includes active ingredients, purpose, warnings, directions, and inactive ingredients. The product is for temporary relief of minor aches and pains of muscles and joints. It contains Menthol 5.64% and Ve Sy 125~ e g. The document includes information about how to use the product safely and contact a Poison Control Center immediately. The other ingredients of the product are Carbomer 934, glyceryl monostearate, PEG-20 sorbitan beeswax, sodium hydroxide, sodium lauryl slifate, and water.*
FDA Label Image

Label3 (Label3)

Label3 (Label3)
This text is a Drug Facts label with information about the active and inactive ingredients, purpose, use, warnings, directions, and other information related to a medication for the temporary relief of minor aches and pains of muscles and joints. The active ingredients for the medication are menthol (5.64%) and Ve Sy 125~ e g. The label cautions the user against applying the medication to wounds or damaged skin, bandaging it tightly, or using it excessively, and advises consulting a doctor if symptoms persist for more than 7 days or if excessive skin irritation develops. The medication is not recommended for children under 3 years of age. Other information includes that it should be stored at temperatures not exceeding 86°F / 30°C.*

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