Instant Hand Sanitizer Gel
Product Images NDC 61010-1111

Product Visual Gallery

This gallery contains 7 technical images submitted to the FDA as part of the official labeling for Instant Hand Sanitizer (NDC 61010-1111). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Safetec Of America, 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

Principal Display Panel – 1.9 L Bottle Label (Saf0n 0003 01)

This is a drug facts label for Safetec Instant Hand Sanitizer enriched with Aloe Vera. It contains 66.5% Ethyl Alcohol and claims to kill 99.9% of bacteria on skin without water or soap. It includes warnings not to use in eyes and to seek medical help if ingested. It is intended for hand washing and should be supervised for children under 6. Its inactive ingredients include aloe vera, carbomer, D&C green #5, D&C yellow #10, fragrance, purified water, triethanolamine. It is manufactured by Safetec of America and comes in a 64 FL.0Z (1.9 L) bottle with reorder no. 17357.*

FDA Label Image

Principal Display Panel – 0.0570 Fl. Oz. Box (Saf0n 0003 02)

This is the description of a hand sanitizer that contains Aloe Vera and kills up to 99.9% of germs. It comes in small packets and is manufactured by Safetec of America Inc. The active ingredient is Aol 55 npic, while the inactive ingredients include yellow 10 vegncs. The product is distributed in boxes containing 100 packets. The text also includes some warnings and directions for use. However, there is some unreadable text present in the document, and it is not possible to provide complete details.*

FDA Label Image

Principal Display Panel – 0.0570 Fl. Oz. Packet (Saf0n 0003 03)

This is a drug facts label for Safetec hand sanitizer. It is an antiseptic that contains 66.5% ethyl alcohol and can be used for handwashing to decrease bacteria on the skin without soap and water. It should only be used externally and is flammable, so it should be kept away from fire or flames and out of reach of children. If the sanitizer gets into the eyes, it should be rinsed thoroughly with water and medical help should be sought if it is ingested.*

FDA Label Image

Principal Display Panel – 2.0 Fl Oz Bottle Panel (Saf0n 0005 04)

This is a product with the National Drug Code (NDC) 61010-1111-0. The name of the product is not available as the text extracted only mentions "Aloe Vera". The content of the package is 2.0 fluid ounces or 59 milliliters.*

FDA Label Image

Principal Display Panel – 4.0 Fl Oz Bottle Panel (Saf0n 0005 05)

This is a product identification code for a medication or a medical device. The NDC number is 61010-1111-1 and the package contains 4.0 fluid ounces or 118 mL of the substance. No details about the medication or device are provided.*

FDA Label Image

Principal Display Panel – 8.0 Fl Oz Bottle Panel (Saf0n 0005 06)

This product is a bottle containing 8.0 fluid ounces (237 milliliters) of a substance enriched with Aloe Vera.*

FDA Label Image

Principal Display Panel – 16.0 Fl Oz Bottle Panel (Saf0n 0005 07)

This is a hand sanitizing product with National Drug Code (NDC) 61010-1111-4. It claims to kill 99.9% of germs and is enriched with Aloe Vera. The product size is 16 fluid ounces (473 ml). However, there is an additional unreadable text "GENGES R ERT" at the bottom, which may not be useful.*

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