Fresh Hand Sanitizer
Product Images NDC 74384-100

Product Visual Gallery

This gallery contains 28 technical images submitted to the FDA as part of the official labeling for Fresh Hand Sanitizer (NDC 74384-100). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Speakeasy Spirits, Llc, 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

Back Label 1000 L Tote (Back Label (01))

This is a hand sanitizer with 80% alcohol that serves as an antiseptic to reduce bacteria that may cause illness. It is intended for use when soap and water are unavailable. The sanitizer should not be used on open wounds or in children under 2 months of age. In case of eye contact, the eyes should be rinsed thoroughly with water. It is flammable and should be kept away from heat or flame. If irritation or rash occurs, a doctor should be consulted, and if swallowed, medical attention should be sought immediately. The hand sanitizer should be placed on hands until dry and stored between 15-30C (59-86F) to prevent freezing or excessive heat. The inactive ingredients include glycerin, hydrogen peroxide, and purified water USP.*

FDA Label Image

Back Label 18.93 L Pail (Back Label (02))

This is a hand sanitizer with 80% alcohol for reducing bacteria that can cause disease. It is intended for use when soap and water are not available. The product contains glycerin, hydrogen peroxide, and purified water as inactive ingredients. The directions state to apply enough product to cover all surfaces of the hands and rub until dry. The hand sanitizer is flammable and should be kept away from heat or flame. It should not be used on open skin wounds or in children less than 2 months of age. If swallowed, medical help should be sought immediately. The product was manufactured according to temporary policies during the COVID-19 pandemic and with only specific USP grade ingredients. Batch and manufacturing date are provided.*

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Back Label 3.785 L Pail (Back Label (03))

This is a hand sanitizer with the active ingredient Alcohol 80% v/v, made to reduce bacteria that may cause disease when soap and water are not available. It is for external use only and is flammable. It should not be used on children under 2 months or on open skin wounds. If there is contact with the eyes, rinse thoroughly. If irritation or rash occurs, discontinue use and seek medical attention. It is made with only United States Pharmacopoeia grade ingredients and should be stored between 15-30C, avoiding freezing or excessive heat above 40C. The inactive ingredients include glycerin, hydrogen peroxide, and purified water USP. The batch number and manufacturing date are also provided.*

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Back Label 1 L Bottle (Back Label (04))

This is a hand sanitizer containing 80% v/v alcohol which is intended to reduce bacteria when soap and water are not available. The product includes warnings for external use only, flammability and to avoid contact with eyes, ears, and mouth. The hand sanitizer contains inactive ingredients such as glycerin, hydrogen peroxide, and purified water USP. The product is manufactured according to a Temporary Policy for Preparation of Certain Alcohol-Based Hand Sanitizer Products During the Public Health Emergency (COVID-19) and the manufacturing date and batch number are provided.*

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Back Label 750 mL Bottle (Back Label (05))

This is a hand sanitizer containing 80% v/v alcohol that helps to reduce bacteria that can cause disease. It is intended for use when soap and water are not available. The product comes with warnings to keep it away from heat or flame, and to keep out of eyes, ears, and mouth. It should not be used on open skin wounds or in children less than 2 months of age. The sanitizer should be rubbed onto the hands until dry. Store it between 15-30C (59-86F) and do not freeze or expose it to excessive heat. The product was manufactured according to the Temporary Policy for Preparation of Certain Alcohol-Based Hand Sanitizer Products During the Public Health Emergency (COVID-19) and contains only United States Pharmacopoeia (USP) grade ingredients. Additional ingredients may impact the quality and potency of the product. The manufacturing date and batch number are provided.*

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Back Label 50 mL Bottle (Back Label (06))

This is a hand sanitizer with 80% v/v alcohol that helps to reduce bacteria that can cause disease. It is suitable for use when soap and water are not available. The product should not be used on open skin wounds or by children under 2 months of age. In case of contact with eyes, rinse thoroughly with water. The product should be rubbed on hands until dry. The hand sanitizer is made with USP-grade ingredients, such as glycerin and hydrogen peroxide, and manufactured according to the Temporary Policy for Preparation of Certain Alcohol-Based Hand Sanitizer Products During the Public Health Emergency caused by COVID-19. Flammable and should be stored below 30°C.*

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Back Label 18.93 L Pail (Back Label (07))

This is a hand sanitizer with an alcohol content of 80% v/v which serves as an antiseptic to help reduce potential disease-causing bacteria. It is meant for external use only and should not be applied on open wounds or ingested. The hand sanitizer should be kept away from heat or flame and is not recommended for children under two months of age. In case of eye contact, rinse thoroughly with water. The sanitizer is made with United States Pharmacopoeia (USP) grade ingredients in compliance with World Health Organization (WHO) recommendations. Other information provided includes storage conditions, directions for use, and the manufacturing date and batch number.*

FDA Label Image

Back Label 3.785 L Pail (Back Label (08))

This is a hand sanitizer with 80% alcohol content, used to reduce bacteria when soap and water are not available. The product should not be used on open skin wounds, in children less than 2 months of age and should be kept away from heat or flame. If there is any irritation or rash, users should stop using and seek medical attention. The hand sanitizer should be stored between 15-30C and should not be frozen or exposed to excessive heat above 40C. The product contains glycerin, hydrogen peroxide, purified water USP, and has been manufactured according to the Temporary Policy for Preparation of Certain Alcohol-Based Hand Sanitizer products During the Public Health Emergency (CoViD-19). No other active or inactive ingredients have been added to the product. Batch number and manufacturing date are available.*

FDA Label Image

Back Label 1 L Bottle (Back Label (09))

This is a hand sanitizer that contains alcohol at 80% v/v that acts as an antiseptic to help reduce the bacteria that can cause disease. It is for external use only and should be kept away from heat or flame. The product should not be used on children less than 2 months of age or on open skin wounds. The user should keep it out of their eyes, ears, and mouth, and in case of contact with the eyes, rinse thoroughly with water. The product should be kept out of reach of children and if swallowed, medical help should be obtained immediately. The hand sanitizer should be sufficiently spread on hands to cover all surfaces and rubbed together until dry. Its inactive ingredients include glycerin, hydrogen peroxide, and purified water USP. The product is manufactured according to the Temporary Policy for Preparation of Certain Alcohol-Based Hand Sanitizer Products during the Public Health Emergency.*

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Back Label 750 mL Bottle (Back Label (10))

This is a hand sanitizer containing 80% v/v Alcohol as an active ingredient aimed to help reduce bacteria that can cause disease. It is not recommended for use on children under 2 months of age and open skin wounds. The product is flammable, must be kept away from heat or flame and should be used externally. If swallowed, get immediate medical attention. The inactive ingredients include glycerin, hydrogen peroxide, and purified water USP. The product is manufactured according to the Temporary Policy for Preparation of Certain Alcohol-Based Hand Sanitizer Products during the Public Health Emergency (COVID-19), and the guidance of the World Health Organization (WHO). Inclusion of different or additional ingredients may impact the quality and potency of the product. Manufacturing date and batch number are provided.*

FDA Label Image

Back Label 4 mL Bottle (Back Label (11))

This is a hand sanitizer that contains 80% Alcohol to reduce bacteria and potentially prevent disease. It is intended for external use only and should be kept away from children, heat, and flame. This product should not be used on open skin wounds or in children under 2 months of age. If contact with eyes, rinse with water. If irritation or rash occurs, discontinue use and seek medical attention. Its inactive ingredients include glycerin, hydrogen peroxide, and purified water USP. It is manufactured and labeled following FDA's guidance to produce certain alcohol-based hand sanitizer products during the COVID-19 pandemic, and other ingredients may affect the quality and potency of the product. The manufacturing date and batch number are specified.*

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Back Label 118 mL Bottle (Back Label (12))

This is a hand sanitizer with 80% alcohol as the active ingredient, used as an antiseptic to help reduce bacteria that can cause disease. It is intended for external use only and should be kept away from heat or flame. The sanitizer should not be used on open skin wounds or in children less than 2 months of age. It is recommended to keep the product out of eyes, ears, and mouth, and rinse thoroughly with water if contact occurs. In case of irritation or rash, stop use and consult a doctor. The sanitizer should be stored between 15-30C (59-86F) and should not freeze or be exposed to excessive heat above 40C (104F). Inactive ingredients include glycerin, hydrogen peroxide, and purified water. This product was manufactured according to the Temporary Policy for Preparation of Certain Alcohol-Based Hand Sanitizer products During the Public Health Emergency. The manufacturing date and batch number are available.*

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Front Label 3.785 L Pail (Fresh 1 Gallon (03))

This is a bottle of hand sanitizer with 80% alcohol antiseptic solution, with a capacity of 1 gallon (3.785 L). The product is made in Nashville and has an NDC code of 74384-100-03. However, it is not suitable for human consumption.*

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Fresh 100ml (14)

This is a description of a hand sanitizer product called Fresh. The product contains 80% Alcohol V/V (ethanol) and is used as an antiseptic to reduce bacteria that can cause disease. It is intended for external use only and should be kept away from heat or flame. When using the product, one should avoid contact with eyes, ears, and mouth. The product comes with warnings to keep out of reach of children and should not be used on open skin wounds. If swallowed, one should contact Poison Control Center right away. The hand sanitizer's inactive ingredients include glycerin, hydrogen peroxide, and purified water USP. The product has only been manufactured with United States Pharmacopoeia (USP) grade ingredients, consistent with World Health Organization (WHO) recommendations for CoViD-19.*

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Fresh 100ml (16)

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Front Label 1 L Bottle (Fresh 1liter (04))

This is a description of a hand sanitizer named "Fresh", manufactured in Nashville. The sanitizer contains 80% alcohol and is a non-sterile topical solution. It comes in a 1-liter bottle and has a National Drug Code (NDC) of 74384-100-04. It is important to note that this product is not intended for human consumption.*

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Fresh 250ml (15)

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Front Label 1000 L Tote (Fresh 264.2 Gallon (01))

This text is a label for a bottle of hand sanitizer. It contains 80% alcohol and is non-sterile. The product is made in Nashville and the bottle size is 264.2 gallons (1000 liters). The National Drug Code (NDC) is 74384-100-01. The label states that the product is not for human consumption.*

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Front Label 18.93 L Pail (Fresh 5 Gallon (02))

This is a 5 gallon (18.93L) container of hand sanitizer produced in Nashville. The solution contains 80% alcohol and is intended for topical use only as an antiseptic. The National Drug Code (NDC) associated with this product is 74384-100-02. It is mentioned that this product is not meant for human consumption. The brand name mentioned is FRESH.*

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Front Label 750 mL Bottle (Fresh 750 mL (05))

FRESH HAND SANITIZER is a non-sterile topical solution that contains 80% alcohol antiseptic. It is made in Nashville and comes in a 750 ML container. The product is not intended for human consumption and has an NDC code of 74384-100-05.*

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Front Label 3.785 L Pail (Pdc 1 Gallon (08))

This is a gallon-sized container of Fresh Hand Sanitizer. It contains a non-sterile, topical solution that is made up of 80% alcohol antiseptic. The NDC number is 74384-100-08. It is manufactured in Nashville by Pickers Vodka. The label indicates that this hand sanitizer is not for human consumption, despite being produced by a company that produces alcoholic beverages.*

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Front Label 1 L Bottle (Pdc 1 Liter (09))

This is a description of a hand sanitizer produced by Pickers Vodka in Nashville, Tennessee. The solution contains 80% alcohol and comes in a 1-liter size with a National Drug Code of 74384-100-09. However, it is stated that the product is not for human consumption.*

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Front Label 4 mL Bottle (Pdc 4ml (11))

Pennington Distilling C@ Hand Sanitizer is an alcohol antiseptic solution that contains 80% alcohol. It is a non-sterile topical solution made in Nashville, Tenn. However, it is not for human consumption.*

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Front Label 18.93 L Pail (Pdc 5 Gallon (07))

This is a hand sanitizer with 80% alcohol that comes in a 5-gallon container. The product is not for human consumption and has been manufactured by Pickers Vodka in Nashville. It is a non-sterile topical solution that can be used to kill germs and reduce the spread of infections. The National Drug Code (NDC) number for this product is 74384-100-07.*

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Front Label 50 mL Bottle (Pdc 50ml (06))

Pennington Distilling Co. has produced a Fresh Hand Sanitizer that contains 80% alcohol antiseptic. It is a non-sterile topical solution that is made in Nashville, Tennessee. The product is not for consumption.*

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Front Label 750 mL Bottle (Pdc 750ml (10))

This is a description of a 750 ml bottle of hand sanitizer with 80% alcohol antiseptic solution. The product is non-sterile and topical. It is made in Nashville and not for human consumption.*

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Front Label 118 mL Bottle (Pdc Sanitizer 4oz)

The text indicates the name of a distillery, "PENNINGTON DISTILLING C9" and that they produce a hand sanitizer named "FRESH". The text also includes a warning that the product is "NOT FOR HUMAN CONSUMPTION".*

FDA Label Image

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