Rezitinas Hand Sanitizer
Product Images NDC 74730-100

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Rezitinas Hand Sanitizer (NDC 74730-100). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Pacific Bridge Products, 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

Rezi3

Labels for REZITINAS Hand Sanitizer moisturizing gel by Pacific Bridge Products, Inc. Each label shows the product name, claims to kill 99.99% of germs, and states it leaves hands soft. Net contents include 1.69 fl. oz. (50 ml), 3.4 fl. oz. (100 ml), 4.0 fl. oz. (118 ml), and 16.0 fl. oz. (472 ml) sizes. All labels include Drug Facts panels listing Ethyl Alcohol 70% as the active ingredient and instructions, warnings, and inactive ingredients.*

FDA Label Image

Rezi4

Labels for REZITINAS Hand Sanitizer moisturizing gel in three sizes: 32 fl. oz. (944 ml), 40 fl. oz. (1.18 L), and 1.69 fl. oz. (50 ml). Each label features the brand name, product name, germ-killing claim, and directions, warnings, uses, active and inactive ingredients. The active ingredient is Ethyl Alcohol 70%, and the product is made by Pacific Bridge Products, Inc.*

FDA Label Image

Rezitins2 (Reziti2)

Label for REZITINAS Hand Sanitizer, a moisturizing gel with 70% ethyl alcohol as the active ingredient. The label highlights that it kills 99.99% of germs and leaves hands soft. The net content is 8.0 fl. oz. (236 mL). The product is marketed by Pacific Bridge Products, Inc., Pomona, CA, and made in China. Drug Facts including uses, warnings, directions, and inactive ingredients are also shown.*

FDA Label Image

Gallon

Drug Facts panel for REZITINAS HAND SANITIZER by Pacific Bridge Products, Inc. It lists ethyl alcohol 70% as the active antiseptic ingredient. The panel includes uses for reducing bacteria, warnings for external use only and flammability, directions for use, and a list of inactive ingredients. The label also has the NDC 74730-100-10 and manufacturer details.*

* 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.