Cc Usa Non-alcohol Foaming Hand Sanitizer
Product Images NDC 75508-005

10 FDA label images from Coil Chem Llc · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 10 technical images submitted to the FDA as part of the official labeling for Cc Usa Non-alcohol Foaming Hand Sanitizer (NDC 75508-005). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Coil Chem Llc, 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

1892.7 mL Half Gallon Label (0.5 Gal Foaming Hs Label)

1892.7 mL Half Gallon Label (0.5 Gal Foaming Hs Label)
Label for CC USA Non-Alcohol Foaming Hand Sanitizer, 0.5 Gallon (1892.7 mL) size, alcohol-free, antimicrobial product with active ingredient Benzalkonium Chloride 0.13%. The label shows directions for use and warnings along with manufacturer Coil Chem LLC contact details and barcode, highlighted by a red, white, and blue theme.*
FDA Label Image

3785.41 mL Gallon Label (1 Gallon Foaming Hs Label)

3785.41 mL Gallon Label (1 Gallon Foaming Hs Label)
Drug Facts panel for CC USA Non-Alcohol Foaming Hand Sanitizer by Coil Chem LLC. Active ingredient: Benzalkonium Chloride 0.13% as antimicrobial. Includes use instructions, inactive ingredients, directions for use, warnings for external use only, and manufacturer contact details. Bottle size is 1 gallon (3785.41 mL).*
FDA Label Image

473.18 mL 16 Oz Label (16 Oz Foaming Hs Label)

473.18 mL 16 Oz Label (16 Oz Foaming Hs Label)
Drug Facts panel for CC USA Non-Alcohol Foaming Hand Sanitizer displays active ingredient benzalkonium chloride 0.13% as antimicrobial. It includes uses for hand washing when soap and water are unavailable. Inactive ingredients list glycerin, decyl glucoside, purified water, aloe vera solution, and citric acid. Directions instruct to apply enough product to hands and rub until dry, supervising children under 6. Warnings note external use only, avoid eyes, stop use if irritation occurs, and keep out of reach of children. Manufacturer contact and website details are also shown.*
FDA Label Image

59.1 mL 2 Oz Label (2 Oz Foaming Hs Label)

59.1 mL 2 Oz Label (2 Oz Foaming Hs Label)
Label for CC USA Non-Alcohol Foaming Hand Sanitizer, 2 oz (59.1 mL), by Coil Chem LLC. The label features a patriotic American flag design with the product name, "Foaming Hand Sanitizer ALCOHOL FREE," and a foaming hand icon. The right side displays Drug Facts including the active ingredient Benzalkonium Chloride 0.13%, directions for use, warnings, manufacturer contact, and a barcode.*
FDA Label Image

999349 mL Tote Label (264 Gal Tote Foaming Hs Label)

999349 mL Tote Label (264 Gal Tote Foaming Hs Label)
Label for CC USA Non-Alcohol Foaming Hand Sanitizer, featuring an American flag design and the statement "Alcohol Free." The product is presented in a 264-gallon tote (999,349 mL). The label includes an antimicrobial active ingredient, benzalkonium chloride 0.13%, and lists glycerin, decyl glucoside, purified water, aloe vera solution, and citric acid as inactive ingredients. Directions and warnings for external use are also visible. Manufactured by Coil Chem LLC in Oklahoma City, OK, with a customer service number and website ccusabest.com.*
FDA Label Image

946.35 mL 32 Oz Label (32 Oz Foaming Hs Label)

946.35 mL 32 Oz Label (32 Oz Foaming Hs Label)
Drug Facts panel for CC USA Non-Alcohol Foaming Hand Sanitizer includes active ingredient benzalkonium chloride 0.13% as an antimicrobial agent. Directions advise covering hands until dry without rinsing and supervising children under 6. Warnings highlight external use only, avoiding eyes, stopping use if irritation occurs, and keeping out of reach of children. Manufactured by Coil Chem LLC in Oklahoma City, OK.*
FDA Label Image

118.3 mL 4 Oz Label (4 Oz Foaming Hs Label)

118.3 mL 4 Oz Label (4 Oz Foaming Hs Label)
Label for CC USA Non-Alcohol Foaming Hand Sanitizer, 4 oz (118.3 mL), alcohol-free. The label features an American flag background and includes the active ingredient Benzalkonium Chloride 0.13%. Manufactured by Coil Chem LLC in Oklahoma City, OK. The label also displays product usage instructions, warnings, and a barcode.*
FDA Label Image

208198 mL Drum Label (55 Gal Foaming Hs Label)

208198 mL Drum Label (55 Gal Foaming Hs Label)
Drug Facts panel for CC USA Non-Alcohol Foaming Hand Sanitizer by Coil Chem LLC. Lists active ingredient benzalkonium chloride 0.13% as antimicrobial. Includes uses for hand washing when soap and water unavailable, inactive ingredients, directions to cover hands until dry, and warnings for external use only, avoiding eyes, supervising children under 6, and stopping use if irritation develops.*
FDA Label Image

177.4 mL 6 Oz Label (6 Oz Foaming Hs Label)

177.4 mL 6 Oz Label (6 Oz Foaming Hs Label)
Label for CC USA Non-Alcohol Foaming Hand Sanitizer, 6 oz (177.4 mL), manufactured by Coil Chem LLC. The label indicates the product is alcohol-free, contains the active ingredient benzalkonium chloride 0.13% as an antimicrobial, and includes ingredient and usage information, warnings, manufacturer contact details, and a barcode.*
FDA Label Image

236.59 mL 8 Oz Label (8 Oz Foaming Hs Label)

236.59 mL 8 Oz Label (8 Oz Foaming Hs Label)
Label for CC USA Non-Alcohol Foaming Hand Sanitizer by Coil Chem LLC, 8 oz (236.59 mL). The label highlights alcohol-free foaming hand sanitizer with a patriotic design featuring the American flag and the CC USA logo. The label also includes Drug Facts, directions for use, warnings, manufacturer contact information, barcode, and product website.*

* 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.