Antibiotic Application Ointment
Product Images NDC 49687-0013

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 Antibiotic Application (NDC 49687-0013). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Cmc Group, 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

Alcohol Cleansing (Alcohol Cleansing)

Alcohol Cleansing (Alcohol Cleansing)
Alcohol Cleansing Pads by DayMark Safety Systems in a 20-pad package. The label shows the product name in English and Spanish (Toallitas Humedas con Alcohol) and indicates the active ingredient as Isopropyl Alcohol, 70%. The label includes usage warnings, storage instructions, and directions for use as a topical antiseptic. The product is made in China and features refill instructions on the side panel, along with a barcode.*
FDA Label Image

Antibiotic Application (Antibiotic Application)

Antibiotic Application (Antibiotic Application)
Packaging label for DayMark Safety Systems Antibiotic Application lotion, featuring refill instructions and a Drug Facts panel detailing active ingredients including bacitracin zinc, neomycin sulfate, and polymyxin B sulfate. The label indicates 10 packs, includes a barcode, and states the product is made in China.*
FDA Label Image

Burn Treatment (Burn Treatment)

Burn Treatment (Burn Treatment)
Drug Facts panel for a burn treatment product by DayMark Safety Systems, including active ingredients benzalkonium chloride 0.13% and lidocaine hydrochloride 0.5%, with uses, warnings, directions, and inactive ingredients. Refill instructions are also shown with illustrations. Packaging states 10 packs made in China.*
FDA Label Image

Eye Wash (Eye Wash)

Eye Wash (Eye Wash)
Packaging label for DayMark Safety Systems Eye Wash, Eye Pads, First Aid Tape Roll 1/2" x 5 yd. The label provides refill instructions, drug facts including active ingredient Purified Water 99.1%, use warnings, directions, storage information, inactive ingredients, and a barcode. The label also displays the product quantity as 1 eye wash, 2 eye pads, and 1 tape, with text in both English and Spanish, and states the product is made in China.*
FDA Label Image

Hand Sanitizer (Hand Sanitizer)

Hand Sanitizer (Hand Sanitizer)
Drug Facts panel from DayMark Safety Systems Hand Sanitizer refill packaging. It lists ethyl alcohol 62% as the active antiseptic ingredient, with uses for handwashing to decrease bacteria and warnings about flammability and external use only. Instructions, storage information, inactive ingredients, refill instructions, and a barcode are also visible on a red background.*
FDA Label Image

Standard (Standard)

Standard (Standard)
Text panel titled SAFETY APPLIED FIRST AID CARRYING CASE listing the contents and refills included in a first aid kit, including bandages, gloves, wipes, hand sanitizer, and pads. The panel references compliance with ANSI/ISEA Z308.1-2015 standards and includes product reorder numbers and quantities for each item. Manufacturer information shows DayMark Safety Systems with a barcode.*
FDA Label Image

Towelettes (Towelettes)

Towelettes (Towelettes)
Packaging label for DayMark Safety Systems Antiseptic Towelettes refill box. The packaging is primarily red with white and black text, indicating 10 wipes per box. It includes refill instructions and a Drug Facts panel listing Benzalkonium Chloride 0.13% as the active ingredient. Barcode and product codes are also present. The label states the product is made in China.*

* 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.