Aloha Gel Hand Sanitizer Pure Peppermint
Product Images NDC 74657-014

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Product Visual Gallery

This gallery contains 6 technical images submitted to the FDA as part of the official labeling for Aloha Gel Hand Sanitizer Pure Peppermint (NDC 74657-014). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Double Body Biotech Limited, 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

74657-010-01; 74657-010-05; 74657-010-10 (74657 010)

74657-010-01; 74657-010-05; 74657-010-10 (74657 010)
This is a drug fact label for a Gel Hand Sanitizer product. It contains 73% Ethyl Alcohol that acts as an antiseptic to reduce bacteria on the skin. It also has Aloe Vera and other inactive ingredients. The product comes in three different sizes, and it is recommended to keep away from flammable sources. The product has been distributed by A.J. & W. Incorporated, based in Honolulu, Hawaii.*
FDA Label Image

74657-011-01 (74657 011)

74657-011-01 (74657 011)
This seems to be a description of a hand sanitizer product labeled as "ALOHA GEL HAND SANITIZER". The product contains 19% alcohol and some other ingredients like Aloe Vera, Glycerin, Propylene Glycol, and fragrances. The directions suggest applying the gel on hands and rubbing until dry. It warns to seek a doctor if irritation occurs and keep it away from children. The barcode and product number are also visible on the label.*
FDA Label Image

74657-012-01 (74657 012)

74657-012-01 (74657 012)
This is a description of a hand sanitizer product labeled "ALOHA GEL HAND SANITIZER" in Tropical Berri flavor. It contains active ingredients such as Wele, Gycern, abomer Propyer, Gl oo Ver Leal, and Fragrance, all approved by FDA. The product comes with a warning to keep away from fire and flames, avoid contact with eyes, swallow, and seek medical attention immediately in case of some side effects. The product can be used without water and should be stored below 105 degrees Fahrenheit. The mentioned batch number is #2020170001.*
FDA Label Image

74657-013-01 (74657 013)

74657-013-01 (74657 013)
This is a drug facts label for Aloha Gel Hand Sanitizer. The active ingredient is 0.5% Aloe Vera. It is used to help reduce bacteria on skin. The warning states to keep away from eyes, not to swallow, and to consult a doctor if rash appears. It is important to keep away from children and to seek immediate medical attention if ingested. The directions instruct to wet hands with the gel and let dry without wiping. The label also contains information on other ingredients including Vitamin E, Carbomer, Propylene Glycol, Aloe Vera Leaf, Fragrance, and a dye called FD&C Yellow No. 5. The label also indicates the product's batch number and expiration date.*
FDA Label Image

74657-014-01 (74657 014)

FDA Label Image

74657-015-01 (74657 015)

74657-015-01 (74657 015)
ALOHA gel hand sanitizer contains 15% alcohol and is intended to help reduce bacteria on the skin. It's important to keep the product away from children and in a cool, dry location. Users should follow the directions by rubbing the sanitizer onto their hands and allowing it to dry. The product's expiration date is 05202022.*

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