Texture Id Anti Dandruff Oil Treatment Oil
Product Images NDC 60717-412

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Texture Id Anti Dandruff Oil Treatment (NDC 60717-412). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Rna Pharma, 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

Active Ingredient (Anti Dandruff Oil Treatment Back Left)

Texture ID Anti Dandruff Oil Treatment topical oil in a blue bottle with a pointed applicator cap. The label shows active ingredient Salicylic Acid 2.0% and includes drug facts, warnings, and additional information about ingredients such as peppermint oil, aloe, and sweet almond oil. It is manufactured for Texture ID by Arcadia Beauty Labs LLC.*

FDA Label Image

Principal Display Area (Anti Dandruff Oil Treatment Front)

Texture ID Anti Dandruff Oil Treatment is a topical oil in a blue plastic bottle with a ribbed screw cap dropper top. The label shows the product name, anti-dandruff indication, and mentions ingredients including salicylic acid. The bottle size is 4 fl oz (120 mL), labeled by RNA PHARMA, LLC.*

FDA Label Image

Inactive Ingredient (Anti Dandruff Oil Treatment Inner Left)

This image shows a continuation of the Drug Facts label on Texture ID Anti Dandruff Oil Treatment, featuring application directions and a detailed list of inactive ingredients. Directions advise applying the oil to dry, itchy scalp using fingertips without rinsing, followed by wrapping hair with a heated towel. Inactive ingredients include various oils, esters, natural extracts, and fragrance components.*

* 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.