Hydroquinone 8%
Product Images NDC 72934-6121

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Hydroquinone 8% (NDC 72934-6121). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Sincerus Florida, 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

X (6121 2 Front)

FDA Label Image

D (6121 2 End)

This is a set of directions for using a product that should be applied externally as directed by a physician. It also includes instructions to wash hands after use and to store the product at a controlled room temperature. A contact number is provided for reporting suspected adverse reactions. The product is not for resale.*

FDA Label Image

S (6121 2 Middle)

This is a description of a medication product. The name of the medication is not specified in the given text. The medication is available only with a prescription. The Lot number of the medication is 1ANOI0ABCOE. The expiration date of the medication is 01/01/1970. The medication contains active ingredient Hydroquinone USP. The medication also contains several inactive ingredients such as Citric Acid USP Anhydrous, Edetate Disodium USP Dihydrate, KOjiCACI, Purified Water, USP, Sodium Chloride USP, and Sodium Metabisulfite NF. The percentage composition of each ingredient is also given, but the quantity of the medication is not mentioned.*

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