Ibarra
Product Images NDC 79577-0007

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Ibarra (NDC 79577-0007). 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)

Drug Facts panel for IBARRA Alcohol Antiseptic 70% Topical Solution hand sanitizer gel. The label lists Ethyl Alcohol 70% v/v as the active antimicrobial ingredient and includes warnings, directions for use, and storage instructions. It also provides inactive ingredients and manufacturer information, indicating the product is made by PROMAQUILA DE COCULA, S.A. DE C.V. in Mexico. The net content is 1000 mL (33.8 fl. oz.).*

FDA Label Image

Label 250 mL (Label 250 mL)

Drug Facts panel for IBARRA Alcohol Antiseptic 70% Topical Solution, a hand sanitizer gel with 250 mL volume. Shows active ingredient ethyl alcohol 70%, use instructions, warnings including flammability and eye contact, directions for use, storage information, and inactive ingredients: water, glycerin, carbomer, aminomethylpropanol, and aloe vera leaf. Manufactured by PROMAQUILA DE COCULA, S.A. DE C.V. in Mexico.*

FDA Label Image

Label 500 mL (Label 500 mL)

Drug Facts panel for IBARRA Alcohol Antiseptic 70% Topical Solution, a hand sanitizer gel non-sterile solution with 500 mL volume. It lists the active ingredient as Ethyl Alcohol 70% v/v with antimicrobial purpose. It includes directions, warnings, uses, and inactive ingredients such as 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.