Luzen Whitening Gel
Product Images NDC 70812-010

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This gallery contains 1 technical images submitted to the FDA as part of the official labeling for Luzen Whitening Gel (NDC 70812-010). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Biostech Co., Ltd., these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

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FDA Label Image

Label (Label)

Label (Label)
This is a drug facts label for a product that contains Hydrogen Peroxide 2.80% (WIW) as an active ingredient. It aids in the removal of phlegm, mucus, or other secretions associated with occasional sore mouth. It is recommended to use up to 2 times daily after meals and at bedtime, and not recommended for children under 13 years of age. The product is for external use only and must be kept out of reach of children. In case of accidental ingestion, medical assistance must be sought immediately. The product must be discontinued and medical help must be sought if symptoms persist or worsen, sore mouth symptoms do not improve in 7 days, or swelling, rash, or fever develops. The inactive ingredients include water, glycerine, PEG400, Ethanol, PVP K29/32 (Povidone), PVP K90 (Povidone), Aerosil 200, Flavor (Applemint HF62184), Citric Acid, Sodium Gitric Acid, Polysorbate 80, Xylitol, Erythritol, and Sucralose. Contact information for questions or comments is also provided.*

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