Ultrasal-er
Product Images NDC 42783-323

View Photos of 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 Ultrasal-er (NDC 42783-323). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Elorac, 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

Ultrasal-5-01.jpg (Ultrasal 5 01)

Ultrasal-5-01.jpg (Ultrasal 5 01)
COOH stands for carboxyl group, which is a functional group composed of a carbon atom double bonded to an oxygen atom and single bonded to a hydroxyl group (-OH). This group is commonly found in organic molecules and plays a significant role in several biochemical processes. For instance, it acts as an acidic group that can easily lose a proton and form a negatively charged carboxylate ion.*
FDA Label Image

Ultrasal-5-04.jpg (Ultrasal 5 04)

FDA Label Image

Ultrasal-5-05.jpg (Ultrasal 5 05)

FDA Label Image

Ultrasal-5-06.jpg (Ultrasal 5 06)

FDA Label Image

Ultrasal-5-07.jpg (Ultrasal 5 07)

FDA Label Image

Ultrasal-bottle-label.jpg (Ultrasal Bottle Label)

Ultrasal-bottle-label.jpg (Ultrasal Bottle Label)
This is a medication for dermatological use only, with instructions to apply once or twice daily, but not to be used in the eyes. It is an Rx only medication and contains "sul D". The package includes information and has an NDC number, and the product is manufactured by Horac, Inc. It seems to have a patent pending and is a wart remover. It comes in a 1300z (10m) package.*
FDA Label Image

Ultrasal-carton-label.jpg (Ultrasal Carton Label)

Ultrasal-carton-label.jpg (Ultrasal Carton Label)
UltraSal-ER is a wart remover solution used for dermatological purposes only. It contains 28.5% salicylic acid in an extended release format and is composed of a film-forming solution containing acrylates copolymer, butyl acetate, carthamus tinctorius seed oil, ethylhexylglycerin, isopropyl alcohol, olea europaea fruit oil, phenic acid, phenoxrelthanol, polysorbate 80, polyvinyl butyral, and pentanyl diisobutyrate. This solution should be used once or twice a day as directed by a healthcare provider and is available only through a prescription. The package insert contains full prescribing information. The solution is flammable and should be kept away from fire or flame. Children should be kept away from it as it is not child-resistant. The bottle should be kept tightly capped and stored at room temperature. The manufacturer is Elorac, Inc, located in Vernon Hills, IL, and it has an additional patent pending.*

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.