Botanif Hand Sanitizer
Product Images NDC 74618-201

7 FDA label images from Gaxtracts Llc · 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 Botanif Hand Sanitizer (NDC 74618-201). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Gaxtracts 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

Botanif 101oz 3000ml

Botanif 101oz 3000ml
Packaging label for Botanif Hand Sanitizer by GAXTRACTS LLC featuring 80% alcohol antiseptic topical solution. The label highlights the product name with instructions for easy opening and dispensing from a 3-liter (101.5 oz) container. The label includes drug facts detailing the active ingredient (Ethyl Alcohol 80%), uses, warnings, storage directions, and inactive ingredients. The design prominently features blue and green colors with the FDA formula compliance seal and a barcode.*
FDA Label Image

Botanif 128oz 3785ml

Botanif 128oz 3785ml
Label for Botanif Hand Sanitizer by GAXTRACTS LLC featuring 80% alcohol antiseptic topical solution in a 1-gallon (3.78 L) container. The label includes use instructions, warnings, and inactive ingredients, along with branding elements stressing bacteria reduction and FDA formula compliance.*
FDA Label Image

Botanif 12oz 354ml

Botanif 12oz 354ml
Drug Facts panel for Botanif Hand Sanitizer with 80% ethyl alcohol as the active ingredient. Includes uses, warnings, directions, and inactive ingredients. Advises external use only, avoiding use on children under 2 months, and keeping out of reach of children. Distributed by Gaxtracts, LLC, with instructions to spray enough to cover hands, rub until dry, and supervise children when using.*
FDA Label Image

Botanif 16oz 473ml

Botanif 16oz 473ml
Drug Facts panel for Botanif Hand Sanitizer with 80% Ethyl Alcohol as active ingredient labeled as antiseptic. It includes sections on uses, warnings, do not use instructions, directions, and other information such as storage conditions and inactive ingredients. The label highlights the product's antiseptic purpose and proper use warnings, including flammability and supervision of children.*
FDA Label Image

Botanif 2oz 59ml

Botanif 2oz 59ml
Label for Botanif Hand Sanitizer by GAXTRACTS LLC showing 80% alcohol content. The label includes drug facts listing Ethyl Alcohol 80% v/v as the active ingredient, usage instructions, warnings, inactive ingredients, and directions. It also highlights key features like spray coverage, dry rub application, and supervision for children. Volume indicated is 2 FL OZ (59 mL).*
FDA Label Image

Botanif 4oz 118ml

Botanif 4oz 118ml
Label of Botanif Hand Sanitizer containing 80% ethyl alcohol as the active ingredient. The label shows the product name, antiseptic purpose, directions for use, warnings, storage information, and inactive ingredients. It is distributed by GAXTRACTS LLC and designed for a 4 FL OZ (118 mL) container. The label also highlights that it reduces bacteria on skin and follows an FDA formula.*
FDA Label Image

236 mL Label (Fdalabel8oz)

236 mL Label (Fdalabel8oz)
Drug Facts panel for Botanif Hand Sanitizer shows ethyl alcohol 80% v/v as the active antimicrobial ingredient, with uses, warnings, and directions for topical application. Inactive ingredients include glycerin, hydrogen peroxide, purified water, and non-sterile solution. The panel includes storage info, usage precautions, and manufacturer branding for GAXTRACTS LLC.*

* 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.