Mini Hand Sanitizer - Orange And Lemon
Product Images NDC 51201-100

3 FDA label images from Goldessence, Limited · 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 Mini Hand Sanitizer - Orange And Lemon (NDC 51201-100). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Goldessence, Limited, 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

Miniorangepanel1 (Miniorange Panel1)

Miniorangepanel1 (Miniorange Panel1)
Drug Facts panel from MINI HAND SANITIZER - ORANGE AND LEMON by Goldessence, Limited showing active ingredient Alcohol 62% as an antiseptic. It states uses for decreasing germs on skin with recommendation for repeated use, and warns for external use only on hands. Includes barcode and manufacturing attribution to Goldessence Limited, New York NY, made in China.*
FDA Label Image

Miniorangepanel2 (Miniorange Panel2)

Miniorangepanel2 (Miniorange Panel2)
Drug Facts panel for MINI HAND SANITIZER - ORANGE AND LEMON by Goldessence, Limited. It includes directions for use, warnings about flammability, cautions to keep out of eyes and reach of children, and instructions on what to do if irritation develops. It also provides other information about storage and potential discoloration, and lists inactive ingredients.*
FDA Label Image

Miniorangepdp (Miniorange Pdp)

Miniorangepdp (Miniorange Pdp)
The label for MINI HAND SANITIZER - ORANGE AND LEMON by Goldessence, Limited shows an orange and lemon fruit graphic background. The text highlights the product name Mini Hand Sanitizer and the scent Orange & Lemon, with a net volume of 1.0 FL. OZ. / 30 ML.*

* 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.