I-max Lightening L
Product Images NDC 42952-203

Product Visual Gallery

This gallery contains 1 technical images submitted to the FDA as part of the official labeling for I-max Lightening L (NDC 42952-203). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Maxlife Usa, 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.

FDA Label Image

Lady-lightening_42952-203-12 (Lady Lightening 203 2013 01 10)

This is a Lightening Cream for intimate areas with an NDC 42952-203-12 code. The cream contains Hydroquinone USP 23 as an active ingredient and is intended for gradual fading of dark areas of the skin. The product is not suitable for use on children under 12 years old, and users should avoid contact with sensitive areas. The instructions recommend applying the cream twice a day, and any adverse reactions should be consulted with a doctor. After 3 months of treatment, the product should be discontinued if there is no noticeable improvement. The formula also contains inactive ingredients such as Alpha Arbutin, Glycerin, and Xanthan Gum. Storage at extreme temperatures should be avoided. For any questions, customers can contact MaxLife USA, Inc by phone or visit their website.*

* 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.