L Bri Klearaway Lotion
Product Images NDC 71238-922

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for L Bri Klearaway (NDC 71238-922). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by L'bri Health & Beauty, 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

Inner Package (Inner Package)

Inner Package (Inner Package)
Label for L BRI Klearaway Blemish Control Lotion, containing 20 mg/mL (2%) salicylic acid as the active ingredient. This topical lotion is for acne treatment and blemish control, suitable for all skin types. The 1 fl oz (30 mL) bottle is formulated with aloe vera, tea tree oil, and various other ingredients. The product is labeled by L'BRI Health & Beauty and made in the USA.*
FDA Label Image

Label0 (Label0)

Label0 (Label0)
Drug Facts panel for L BRI Klearaway Blemish Control Lotion, listing Salicylic Acid 2.0% as the active ingredient for acne treatment. It includes use instructions, external use warnings, storage directions, and a detailed list of inactive ingredients. Also shows manufacturing origin, contact info, animal testing status, recycling icons, and a barcode.*
FDA Label Image

Outer Package (Outer Package)

Outer Package (Outer Package)
Packaging label for L BRI Klearaway Blemish Control Lotion, topical lotion containing Salicylic Acid 20 mg/mL. The label is light green with white and black text, displaying the product name, usage as a blemish control lotion for all skin types, and a 1 fl oz (30 mL) volume. The label includes a detailed Drug Facts panel and states it is formulated exclusively for L'BRI Health & Beauty.*

* 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.