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)

I-MAX LIGHTENING L Lightening Cream packaging label with NDC 42952-203-12, containing 2 oz (59 g) of cream for intimate area use. The active ingredient is Hydroquinone USP 2%. Labeler is MAXLIFE USA, INC., located in Los Angeles, CA. The label highlights use for gradual fading of dark skin areas and lists detailed directions, warnings, and inactive ingredients.*

* 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.