Hand Sanitizer Gel
Product Images NDC 67777-911

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 Hand Sanitizer (NDC 67777-911). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Dynarex Corporation, 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

1427_bx_master (1427 Bx Master R250919 3)

1427_bx_master (1427 Bx Master R250919 3)
Packaging label for Dynarex Safety Hand Sanitizer gel with Moisturizing Aloe, 1 fl. oz. (29.5 mL) flip top square bottles, in a 24-count pack. The label features the Dynarex Safety logo, an aloe graphic, and states it kills more than 99.99% of germs. It includes a Drug Facts panel, barcode, and manufacturer information for Dynarex Corporation.*
FDA Label Image

1428_bx_master (1428 Bx Master R250919 3)

1428_bx_master (1428 Bx Master R250919 3)
Carton packaging for Dyna Safety Hand Sanitizer gel with moisturizing aloe, labeled as 2 fl. oz. (59 mL) flip-top square bottles. The package design features the brand name, product name, aloe leaf image, and states it kills more than 99.99% of germs. The labeler is Dynarex Corporation, and the Drug Facts panel is included with active ingredient and usage information.*
FDA Label Image

1429_bx_master (1429 Bx Master R250919 4)

1429_bx_master (1429 Bx Master R250919 4)
Packaging label for Dynarex Safety Hand Sanitizer gel with Moisturizing Aloe. The front panel displays the brand and product name, emphasizing moisturizing aloe, with net contents of 4 fl. oz. (118.3 mL). The label includes a drug facts panel, barcode, and manufacturer information for Dynarex Corporation. The product claims to kill more than 99.99% of germs and is for topical use.*
FDA Label Image

1431_in_master (1431 In Master R250919 4)

1431_in_master (1431 In Master R250919 4)
Label for Dynarex Corporation Hand Sanitizer, a topical gel with 70% alcohol active ingredient. The label highlights moisturizing aloe, antiseptic handwash purpose, warnings for external use only, and storage instructions. The product size is 8 fl. oz. (236.5 mL) with NDC 67777-911-10, and it is made in China.*
FDA Label Image

1432_in_master (1432 In Master R250922 2)

1432_in_master (1432 In Master R250922 2)
Label for Dynarex DynaSafety Hand Sanitizer gel with moisturizing aloe, containing 70% alcohol. The front highlights 16 fl oz (473 mL) volume and claims to kill more than 99.99% of germs. The back includes drug facts, warnings, directions, inactive ingredients, and manufacturer information for Dynarex Corporation.*
FDA Label Image

1433ub-10_bx_master (1433ub 10 Bx Master R250922 4)

1433ub-10_bx_master (1433ub 10 Bx Master R250922 4)
Dynarex Corporation Hand Sanitizer with Moisturizing Aloe gel label for a 10-pack of 0.9 g packets. The active ingredient is 70% v/v alcohol as an antiseptic handwash. The label includes Drug Facts with warnings, directions, inactive ingredients, and storage instructions. The packaging highlights DynaSafety branding and the NDC 67777-911-16.*
FDA Label Image

1433_bx_master (1433 Bx Master R250922 3)

1433_bx_master (1433 Bx Master R250922 3)
Packaging label for Dyna Safety Hand Sanitizer gel with moisturizing aloe. The label displays the product name, active ingredient concentration of 70% alcohol, and packaging information indicating 144 packets each with 0.9 gram (1.01 mL) net weight. The label includes drug facts, directions, warnings, inactive ingredients, and manufacturer details for Dynarex Corporation. The label also features a barcode, NDC number 67777-911-14, and an aloe image graphic.*

* 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.