Ibarra
Product Images NDC 79577-0006

3 FDA label images from Promaquila De Cocula, S.a. De C.v. · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Ibarra (NDC 79577-0006). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Promaquila De Cocula, S.a. De C.v., 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

Label 1000 mL (Label 1000 mL)

Label 1000 mL (Label 1000 mL)
Drug Facts panel for IBARRA Alcohol Antiseptic 70% topical solution hand sanitizer gel. The active ingredient is Ethyl Alcohol 70% v/v with antimicrobial purpose. The label includes use instructions, warnings, directions, and storage information. The product volume is 1000 mL (33.8 fl. oz.). Manufacturer is PROMAQUILA DE COCULA, S.A. DE C.V. in Mexico.*
FDA Label Image

Label 250 mL (Label 250 mL)

Label 250 mL (Label 250 mL)
Drug Facts panel for IBARRA Hand Sanitizer Gel, a 70% ethyl alcohol topical solution. The label includes active ingredient and antimicrobial purpose, usage instructions for hand sanitizing, warnings about flammability and safe use, directions for application, storage temperature, inactive ingredients, and manufacturer details. Net contents are 250 mL (8.45 fl. oz).*
FDA Label Image

Label 500 mL (Label 500 mL)

Label 500 mL (Label 500 mL)
Drug Facts panel for IBARRA Alcohol Antiseptic 70% Topical Solution hand sanitizer gel, 500 mL (16.9 fl. oz.). Lists active ingredient as Ethyl Alcohol 70% v/v with antimicrobial purpose. Includes uses, warnings, directions, storage information, and inactive ingredients like water, glycerin, carbomer, aminomethylpropanol, and aloe vera leaf.*

* 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.