Hand Sanitizer
Product Images NDC 74988-730

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 8 technical images submitted to the FDA as part of the official labeling for Hand Sanitizer (NDC 74988-730). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Sanitizenow Inc., 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

Updated Purrexx Label 1041 L (275 Gal) 80 V2

Updated Purrexx Label 1041 L (275 Gal) 80  V2
This is a description of a hand sanitizer manufactured in the USA. It contains 80% alcohol, which is meant to reduce bacteria that potentially can cause diseases. This product is for external use only, and it is flammable. It comes with instructions including directions for use, warnings, and other important information. The inactive ingredients include Water, Hydrogen Peroside, Glycerin, Carbomer 1342, Aloe VeraLeaf, FD&C Blue No. 1, FDSC Yellow No, 5, Alpha Tocopherol Acetate, and Fragrance. The sanitizer is said to contain plant extracts and skin conditioner, which kills about 99.99% of germs. The product is an FDA registered item and comes in a 1041L (275 Gal) container.*
FDA Label Image

Updated Purrexx Label 16 Oz (473 mL) 80 V2

Updated Purrexx Label 16 Oz (473 mL) 80  V2
This is a description of a hand sanitizer with the brand name "High Potency Hand Sanitizer". The sanitizer is manufactured and bottled in the USA. It is FDA registered and contains active ingredients such as Hydogenboris, Gy Caoaer 1545, and Ao Vs Lot. The sanitizer is said to kill 99.99% of germs and comes in a 473 mL (16 oz) dispenser bottle. The usage directions instruct to dispense the sanitizer on hands and rub hands together until all surfaces are covered. Other information includes the storage and pricing details.*
FDA Label Image

Updated Purrexx Label 2 Oz (59 mL) 80 V2

Updated Purrexx Label 2 Oz (59 mL) 80  V2
This is a description of a hand sanitizer product that is FDA registered and manufactured in the USA. The product claims to contain plant extracts and a skin conditioner, and it has active ingredients that kill 99.99% of germs. The directions for use include rubbing the product into the hands, covering all surfaces until the hands are dry. The product warns to keep out of reach of children and to seek medical help if swallowed.*
FDA Label Image

Updated Purrexx Label 208 L (55 Gal) 80 V2

Updated Purrexx Label 208 L (55 Gal) 80  V2
This is a hand sanitizer with 80% alcohol that aims to reduce bacteria that can cause disease. It is flammable and should be kept away from heat sources. The product should not be used on open wounds or children under 2 months of age. It should be kept away from the eyes, ears, and mouth. If irritation or rash occurs, it is advisable to stop using it and seek a doctor's advice. The product should be stored between 15-30C and kept away from freezing and excessive heat above 40C. It is made in the USA and registered by the FDA. Its active and inactive ingredients are given, and it is packaged in 208L (55Gal).*
FDA Label Image

Updated Purrexx Label 25741 L (6800 Gal) 80 V2

Updated Purrexx Label 25741 L (6800 Gal) 80  V2
This is a description of an alcohol-based hand sanitizer that contains 80% alcohol to reduce bacteria and the risk of infection when soap and water are not available. It contains inactive ingredients such as water, hydrogen peroxide, aloe vera leaf, carbomer 1342, FD&C Blue No. 1, FD&C Yellow No. 5, alpha-tocopherol acetate, and fragrance that are used to make the sanitizer. This sanitizer should be used externally and is flammable. Users should avoid contact with eyes, ears, mouth, and open skin wounds, and keep it out of the reach of children. In case of ingestion, medical attention is needed right away. The product should be stored in a cool place and not frozen or exposed to excessive heat. The sanitizer is manufactured in the USA, registered with FDA, and kills 99.99% of germs.*
FDA Label Image

Updated Purrexx Label 3.79 L (1 Gal) 80 V2

Updated Purrexx Label 3.79 L (1 Gal) 80  V2
This is a drug facts label for a hand sanitizer product with a volume of 3.79L, manufactured and bottled in the USA. It is made with plant extracts and a skin conditioner, and contains 80% alcohol as an antiseptic. The hand sanitizer is intended for use in reducing bacteria and germs on hands when soap and water are not readily available. The label provides directions for use and safety precautions, including warnings such as flammability and advice to keep the product out of eyes, ears, and mouth. The hand sanitizer is not intended for use on open skin wounds, in children less than 2 months of age, or on irritated skin. The inactive ingredients, stored at temperatures between 15-30C, include water, hydrogen peroxide, and aloe vera leaf extract.*
FDA Label Image

Updated Purrexx Label 4 Oz (118 mL) 80 V2

Updated Purrexx Label 4 Oz (118 mL) 80  V2
This text appears to be a mixture of multiple product labels and instructions. It mentions a hand sanitizer that is manufactured and bottled in the USA and is meant to kill 99.99% of germs. The hand sanitizer contains high potency and is made with plant extracts and a skin conditioner. It comes in a 4oz (118mL) bottle with NDC: 74988-730-40. There are also references to FDA registration and directions on how to apply the hand sanitizer. Some of the text is not readable, and there are no clear instructions or descriptions for any other products mentioned.*
FDA Label Image

Updated Purrexx Label 8oz (236ml) 80 V2

Updated Purrexx Label 8oz (236ml) 80  V2
This is a description for a hand sanitizer product. The name of the product is High Potency Hand Sanitizer and it is made with plant extracts and contains skin conditioner. The product claims to kill 99.99% of germs. The bottle size is 8oz (236 mL). The directions tell the user to dispense hand sanitizer on the palm of their hand and rub their hands together for at least 20 seconds or until hands feel dry. The product is FDA registered with the NDC number 74988-730-80. There is also a warning to keep the product away from children and to stop using it if there are any adverse reactions or if a visit to the doctor is required.*

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