Hand Sanitizer
Product Images NDC 74976-800

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 6 technical images submitted to the FDA as part of the official labeling for Hand Sanitizer (NDC 74976-800). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Innova4d Usa Corp, 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

1000 mL Back Label (I4d 80 1000 mL Back Label)

1000 mL Back Label (I4d 80 1000 mL Back Label)
This is a description of a hand sanitizer with 80% alcohol content, used for antiseptic purposes to help reduce the spread of bacteria that cause disease. It comes with a warning to keep away from children and flame, and not to use on open skin wounds, among other warnings. To use, an individual should place enough product on the hands to cover all surfaces and rub them together until dry. The inactive ingredients are glycerin, hydrogen peroxide, and purified water USP. It is manufactured by InnovadD USA CORP and comes in a 15-30°C temperature range. Furthermore, it has an NDC 74976-787-10 identification number.*
FDA Label Image

1000 mL Front Label (I4d 80 1000 mL Front Label)

1000 mL Front Label (I4d 80 1000 mL Front Label)
This is a hand sanitizer solution made in an FDA registered facility with Isopropyl Alcohol Antiseptic 75% and approved formula by the World Health Organization. It is a non-sterile topical solution.*
FDA Label Image

300 mL Back Label (I4d 80 300 mL Back Label)

300 mL Back Label (I4d 80 300 mL Back Label)
This is a Drug Facts label for a hand sanitizer containing 80% alcohol as an antiseptic to help reduce bacteria that potentially cause diseases. The directions indicate that enough product must be placed on hands to cover all surfaces, and hands must be rubbed together until dry. It is essential to keep this product out of eyes, ears, and mouth, and away from heat or flame. Also, the label warns that the product must not be consumed and should not be used on open skin wounds or in children under two months of age. If irritation or rash occurs, stop use immediately and contact a doctor since these may be symptoms of a severe condition. The hand sanitizer contains glycerin, hydrogen peroxide, and purified water USP as inactive ingredients, and it is manufactured by InnovadD USA CORP.*
FDA Label Image

300 mL Front Label (I4d 80 300 mL Front Label)

300 mL Front Label (I4d 80 300 mL Front Label)
This is a description for a hand sanitizer product that is a topical solution with 80% alcohol as the active ingredient. The formula is approved by the World Health Organization, and it is made in an FDA registered facility. The solution is non-sterile.*
FDA Label Image

4546 mL Back Label (I4d 80 Back Label)

4546 mL Back Label (I4d 80 Back Label)
This is a drug facts label for a hand sanitizer produced by InnovadD USA CORP. It contains 80% v/v of alcohol which helps to reduce bacteria and has an antiseptic purpose. The sanitizer is intended for use when soap and water are not available. However, it should not be used on open skin wounds, on children below 2 months, or near the mouth, eyes and ears. If it comes into contact with eyes, rinse immediately with water. Children under six should be supervised when using it to avoid swallowing. It should be stored between 15-30°C, kept away from heat and flames, and not frozen. The sanitizer also includes inactive ingredients such as glycerin and hydrogen peroxide. The label also contains the manufacturing address and NDC number.*
FDA Label Image

4546 mL Front Label (I4d 80 Front Label)

4546 mL Front Label (I4d 80 Front Label)
This is a hand sanitizer solution that contains 80% alcohol and is approved by the World Health Organization. It comes in a non-sterile solution and is made in a facility registered by the FDA. The solution is in a 128 fl oz (1-gallon) container.*

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