Alcohol Free Foaming Hand Sanitizer Soap
Product Images NDC 65601-700

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Product Visual Gallery

This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Alcohol Free Foaming Hand Sanitizer (NDC 65601-700). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Betco Corporation, 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

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This is a drug facts label for an alcohol-free foaming hand sanitizer. The active ingredient is benzalkonium chloride at 0.13% and it is an antiseptic. The product is intended to reduce microorganisms on the skin when soap and water are not available. The label provides warnings, including to avoid contact with eyes and to discontinue use if irritation or redness develops. The directions state to dispense 2 pumps of the product onto the palm of the hand and rub thoroughly until dry. The label also includes information on inactive ingredients. There is some text in Spanish, but it is unclear if it is a translation of the English text or additional information.*
FDA Label Image

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This is a hand sanitizer product that contains 0.13% of Benzalkonium Chloride, which works as an antiseptic. It is used as a substitute for soap and water when they are not available. The product is not to be used internally and contact with eyes should be avoided. In case of ingestion, medical assistance is needed immediately. Users should thoroughly rub the product on both hands until it dries, and it is recommended to read the entire label before usage. The product is manufactured by Betco Corporation, located in Bowling Green, Ohio, USA. The inactive ingredients include Deionized Water, Sodium PCA, PEG/PPG-8/3 Laurate, Dimethicone, PEG-3 Cocamide, Fragrance, Magnesium Salts, Methyl Chloro Isothiazolinone, Methyl Isathiazolinone, D&C Green 45, and it is alcohol-free.*
FDA Label Image

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This is a Drug Facts label for a 50 mL (1.69 fl. oz.) Alcohol-Free Foaming Hand Sanitizer that contains benzalkonium chloride 0.13% as an antiseptic. The hand sanitizer is designed to reduce microorganisms on the skin and can be used when soap and water are not available. It contains several inactive ingredients, including Detorized Water, Sodium PCA, PEGIPPG-8/3, Laureth-3, PEG-3 Cocamide, Fragrance, Magnesium Nitrate, and DAC Green 45. The product carries warnings for external use only, avoiding contact with eyes, and consulting a physician if irritation persists for more than 72 hours. In case of ingestion, medical help or contacting Poison Control Center is advised. It is made in the USA and the property rights are reserved by Betoo Corporation.*
FDA Label Image

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This is a foaming hand sanitizer that is alcohol-free and contains Benzalkonium Chloride as an active ingredient. It can be used to reduce microorganisms on the skin when soap and water are not available. The sanitizer should be applied to the palms and rubbed thoroughly over all surfaces of both hands until dry. The product is for external use only and should be kept out of reach of children. If swallowed, medical help should be sought immediately. Inactive ingredients include deionized water, Sodium PCA, PEG/PPG-8/3 Laurate, Dimethicone, PEG-3 Cocamide, Fragrance, Magnesium Salts, Methyl Chloro Isothiazolinone, Methyl Isothiazolinone, and D&C Green #5. Drug and Product facts, warnings, and instructions are also listed.*
FDA Label Image

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This is a Drug Facts label for a Hand Sanitizer from Betco Corporation. It is an alcohol-free foaming hand sanitizer intended to reduce microorganisms on the skin when soap and water are not available. The active ingredient is Benzalkonium Chloride. The user should keep the product out of reach of children, read the entire label before use, cover hands thoroughly with the product, and rub hands together until dry. The inactive ingredients include deionized water, Magnesium Sats, sodium PCA, PEG/PPG-8/3 Laurate, Dimethicone, PEG-3 Cocamide, Fregrance, Methyl Chioro lsathiazolinone, Methy kothizzolinane, DEC Green #5. The product label contains warnings, precautions and instructions for use, and contact information in case of questions.*

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