Instant Hand Sanitizer Gel
Product Images NDC 61010-1111

View Photos of Packaging, Regulatory Labels, and Product Appearance

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)

Principal Display Panel – 1.9 L Bottle Label (Saf0n 0003 01)
Label for Instant Hand Sanitizer gel containing alcohol, manufactured by Safetec of America, Inc. It features a mostly blue and green color scheme, states the product kills 99.9% of germs and is enriched with aloe vera. The label includes drug facts with ethyl alcohol 66.5% as the active antiseptic ingredient, along with warnings, directions, and inactive ingredients. The product volume is 64 fluid ounces (1.9 L).*
FDA Label Image

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

Principal Display Panel – 0.0570 Fl. Oz. Box (Saf0n 0003 02)
Instant Hand Sanitizer gel by Safetec of America, Inc. The label shows 0.0570 FL. OZ. (1.68 ML) packets, 100 packets per box. It features a fresh scent and claims to kill 99.9% of germs, enriched with aloe vera. The packaging highlights the product as an antiseptic for topical use with ethyl alcohol 66.5% as the active ingredient.*
FDA Label Image

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

Principal Display Panel – 0.0570 Fl. Oz. Packet (Saf0n 0003 03)
Drug Facts panel for Instant Hand Sanitizer gel with active ingredient ethyl alcohol 66.5% as an antiseptic. Includes usage instructions for handwashing, warnings about external use, flammability, and ingestion, directions to wet hands and wrists thoroughly and let dry, and lists inactive ingredients such as aloe vera and carbomer. Manufactured by Safetec of America, Inc.*
FDA Label Image

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

Principal Display Panel – 2.0 Fl Oz Bottle Panel (Saf0n 0005 04)
Label for Safetec Instant Hand Sanitizer Gel, 2.0 fluid ounces (59 mL). Features claims of killing 99.9% of germs and being enriched with aloe vera. The label includes a logo indicating compliance with CDC handwashing recommendations. The product is a topical gel.*
FDA Label Image

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

Principal Display Panel – 4.0 Fl Oz Bottle Panel (Saf0n 0005 05)
Label for Safetec Instant Hand Sanitizer gel, 4.0 fl. oz. (118 ml) bottle. The label highlights it kills 99.9% of germs and is enriched with Aloe Vera. The design includes a blue and green gradient background with a water droplet graphic and mentions adherence to CDC handwashing recommendations.*
FDA Label Image

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

Principal Display Panel – 8.0 Fl Oz Bottle Panel (Saf0n 0005 06)
Packaging label for Safetec Instant Hand Sanitizer gel, containing alcohol at 540.26 g/L strength. The label highlights it kills 99.9% of germs and is enriched with Aloe Vera. The product volume is 8.0 fluid ounces (237 mL) and it is marketed by Safetec of America, Inc. The label features a blue and white color scheme with a water drop graphic and the word 'Fresh'.*
FDA Label Image

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

Principal Display Panel – 16.0 Fl Oz Bottle Panel (Saf0n 0005 07)
Label for Safetec Instant Hand Sanitizer gel with 540.26 g/L alcohol strength. The label highlights the product kills 99.9% of germs and is enriched with aloe vera. It features a blue gradient background with a water droplet splash image, the Safetec logo, and states the volume as 16 FL. OZ. (473 mL).*

* About these descriptions: Image descriptions on this page are generated by automated AI analysis of the product label images from the manufacturer's FDA label submission (SPL). They are provided for reference only and may contain errors or omissions. Always rely on the printed label itself and the official FDA labeling, and consult a pharmacist or healthcare professional with any questions about this product.