Hand Sanitizer
Product Images NDC 74092-280

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Hand Sanitizer (NDC 74092-280). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Caribbean Distillers 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

1.5l Plastic (1.5l Plastic)

1.5l Plastic (1.5l Plastic)
CD Caribbean Distillers have manufactured alcohol antiseptic 80% topical solution for use as a hand sanitizer to reduce the bacteria that potentially can cause diseases. This non-sterile, non-potable solution contains denatured ethyl alcohol, glycerin and hydrogen peroxide. It has to be kept away from heat or flame, eyes, ears, mouth, young children under 2 months, and open skin wounds. In case of contact with eyes, rinse eyes thoroughly with water. Supervise children under 6 years of age while using to avoid swallowing. If irritation or rash occurs, stop using the product and consult a doctor. The sanitizer should be stored between 15-30°C (59-86°F), avoided from excessive heat above 40°C (104°F) or freezing. The product has been manufactured by Caribbean Distillers, LLC in Auburndale, FL.*
FDA Label Image

1.75 L Plastic (1.75l Plastic)

FDA Label Image

1003.13 L Drum (1003.13 L Drum)

1003.13 L Drum (1003.13 L Drum)
This is a Drug Facts label for an alcohol antiseptic 80% topical solution hand sanitizer produced by Caribbean Distillers, LLC located in Auburndale, Florida. The product is used to reduce bacteria that can potentially cause disease when soap and water are not available. The bottle contains 265 gallons, which is equivalent to 1,003,134.12276 mL, and is intended for consumer use only. The label includes directions on how to use the product, warnings, and precautions. Inactive ingredients include glycerin, hydrogen peroxide, and purified water USP.*
FDA Label Image

1l Plastic (1l Plastic)

FDA Label Image

208.198 L Drum (208.198 L Drum)

208.198 L Drum (208.198 L Drum)
This is a Drug Fact label for a hand sanitizer manufactured by Caribbean Distillers LLC in Florida. It is a Non-sterile Solution containing 80% Alcohol Antiseptic with a National Drug Code of 74092-280-04. The product is intended for consumer use to help reduce bacteria potentially causing diseases when soap and water are not available. This hand sanitizer is flammable and should be kept away from heat or flame. Users should avoid using it on open skin wounds, or in children under 2 months old. In case of contact with eyes, rinse thoroughly with water. Users who experience rash, irritation, or any sign of a serious condition should stop the use of the product and contact a physician. It is important to store the hand sanitizer between 15-30C (59-86F) to prevent freezing and excessive heat above 40C (104F). The inactive ingredients include glycerin, hydrogen peroxide, and purified water USP.*

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