Sera Hand-sanitizing Wipe
Product Images NDC 77822-201

2 FDA label images from Sng Co., Ltd · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Sera Hand-sanitizing Wipe (NDC 77822-201). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Sng 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.

Product Images & Figures Index

FDA Label Image

280g Ndc: 77748-201-02 Label (Sera Hand Sanitizing Wipe 280g Label)

280g Ndc: 77748-201-02 Label (Sera Hand Sanitizing Wipe 280g Label)
SERA Hand-Sanitizing Wipe packaging label from SNG CO., LTD features a white plastic container with a flip-top lid. The front displays the SNG logo and product name in blue and green. The label includes product use details, directions, warnings, drug facts with active ingredient benzalkonium chloride 0.1%, ingredients, storage instructions, and the manufacturer address in Korea. The label highlights that the wipes help reduce bacteria and provides safety and usage information.*
FDA Label Image

42g Ndc: 77748-201-01 Label (Sera Hand Sanitizing Wipe 42g Label)

42g Ndc: 77748-201-01 Label (Sera Hand Sanitizing Wipe 42g Label)
SERA Hand Sanitizing Wipe packaging label from SNG CO., LTD. The label highlights the product name and a shield icon indicating 99.9% hard wash efficacy. It includes usage directions, a 7-step hydrostatic process for purification, warnings, and drug facts. The active ingredient is benzalkonium chloride 0.1%, with other ingredients listed. The product is made in Korea and comes in a 42g pack containing 10 sheets.*

* 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.