Barton And Fitz
Product Images NDC 77464-0001

Product Visual Gallery

This gallery contains 8 technical images submitted to the FDA as part of the official labeling for Barton And Fitz (NDC 77464-0001). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Varsity Distilled Spirits 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

354 mL Label (Production Barton Fitz 2x3 Labels V2 12 Oz 01)

The label for Barton & Fitz hand sanitizer by Varsity Distilled Spirits LLC features the brand name prominently. It is labeled as scent-free hand sanitizer, produced in Austin, Texas. The product is a topical solution containing 80% alcohol antiseptic in a 1.2 fl oz (354 mL) container. The label emphasizes it is a non-sterile solution.*

FDA Label Image

473 mL Label (Production Barton Fitz 2x3 Labels V2 16 Oz 01)

Barton and Fitz hand sanitizer label from Varsity Distilled Spirits LLC. The label states the product is scent-free, made in Austin, TX, and contains 16 fluid ounces (473 mL). It is described as a topical solution with 80% alcohol antiseptic, a non-sterile solution. The logo and product name are prominently displayed.*

FDA Label Image

236 mL Label (Production Barton Fitz 2x3 Labels V2 8 Oz 01 2)

Label for Barton and Fitz hand sanitizer by Varsity Distilled Spirits LLC. The product is scent free and made in Texas. It contains 8 fl oz (236 mL) of topical solution with 80% alcohol antiseptic. The label also states it is a non-sterile solution.*

FDA Label Image

946 mL Label (Production Barton Fitz 3x4 Labels V2 32 Oz 01)

The packaging label for Barton and Fitz Hand Sanitizer, scent free, contains 32 fluid ounces (946 mL) of topical solution with 80% alcohol antiseptic. It is labeled as a non-sterile solution made in Texas and produced by Varsity Distilled Spirits LLC.*

FDA Label Image

354 mL Back (Production Barton Fitz Back 2x3 Labels V2 12 Oz 01)

Drug Facts panel for Barton and Fitz by Varsity Distilled Spirits LLC, showing active ingredient as alcohol 80% v/v. The panel includes warnings about flammability, advises external use only, and directions to rub hands together until dry, with supervision for children under six. Other information covers storage temperatures and lists inactive ingredients hydrogen peroxide, glycerin, and purified water.*

FDA Label Image

473 mL Back (Production Barton Fitz Back 2x3 Labels V2 16 Oz 01)

Drug Facts panel for Barton and Fitz antiseptic alcohol 80% v/v, listing active ingredient, warnings including flammability and use restrictions, directions for use, inactive ingredients (hydrogen peroxide, glycerin, purified water), storage instructions, and distributor information by Varsity Distilled Spirits LLC in Austin, TX.*

FDA Label Image

236 mL Back (Production Barton Fitz Back 2x3 Labels V2 8 Oz 01)

Drug Facts panel for Barton and Fitz antiseptic with 80% v/v alcohol active ingredient. The panel includes warnings about external use only, flammability, and keeping out of children’s reach. Directions advise placing enough product on hands to cover all surfaces and supervising children under 6. Other information covers storage temperature and avoidance of excessive heat. Inactive ingredients listed are hydrogen peroxide, glycerin, and purified water.*

FDA Label Image

946 mL Back (Production Barton Fitz Back 3x4 Labels V2 32 Oz 01)

Drug Facts for Barton and Fitz show it is an antiseptic with alcohol 80% v/v as the active ingredient. It is for external use only and flammable. Warnings include keeping away from children and fire, and directions emphasize placing enough product on hands and rubbing until dry. Additional info covers storage conditions and inactive ingredients such as hydrogen peroxide, glycerin, and purified water.*

* 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.