Dermeleve Cream
Product Images NDC 81507-002

Product Visual Gallery

This gallery contains 16 technical images submitted to the FDA as part of the official labeling for Dermeleve (NDC 81507-002). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Advanced Derm Solutions 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

Image Description (Label 80g 1)

Drug Facts panel for Dermeleve Cream containing Aluminum Acetate 0.2% as the active ingredient. The panel lists uses such as treating insect bites, minor burns, athlete's foot, and rashes caused by soaps or cosmetics. Warnings include external use only, avoiding contact with eyes, and not applying to open wounds. Directions specify use for adults and children over two years. The inactive ingredients and manufacturer information for Advanced Derm Solutions LLC are also provided.*

FDA Label Image

Image Description (Label 80gm 2)

Dermeleve 0.2% Aluminum Acetate topical cream label from Advanced Derm Solutions LLC. The label highlights the product as a steroid-free, soothing cream designed to relieve dry, itchy, and irritated skin while helping retain moisture and aid skin barrier function. It contains Aluminum Acetate, Strontium Mineral Salts, Ceramides, Hyaluronic Acid, Shea Butter, and Vitamins C+E. The net weight is 80g and it is made in the USA.*

FDA Label Image

Image Description (Label 30g 1)

Front label of Dermeleve Soothing Cream featuring Aluminum Acetate 0.2% topical cream. The label highlights relief for dry, itchy, and irritated skin, notes that it is steroid-free, and lists additional ingredients such as strontium mineral salts, ceramides, hyaluronic acid, shea butter, and vitamins C and E. The cream is manufactured by Advanced Derm Solutions LLC and comes in a 30g package made in the USA.*

FDA Label Image

Image Description (Label 30g 2)

Drug Facts label panel for Dermeleve Cream containing Aluminum Acetate 0.2% as active ingredient with astringent purpose. The label lists uses such as relief of minor skin irritations and warnings for external use, eye contact, and application on open wounds. Directions specify use for adults and children two years and older. Inactive ingredients and manufacturer details of Advanced Derm Solutions LLC are included.*

FDA Label Image

Image Description (Label 30g 3)

Label panel for Dermeleve Advanced Formula Soothing Cream, a topical cream containing Aluminum Acetate by Advanced Derm Solutions LLC. The label highlights the cream's use for dry and itchy skin, listing SrX-38, a proprietary blend with Aluminum Acetate and other ingredients to reduce irritation and enhance skin barrier. The net weight is 30 grams, and the product is made in the USA.*

FDA Label Image

Image Description (Label 30g 4)

Dermeleve Soothing Cream packaging label showing product name and usage note. The label indicates it is for all skin types and mentions topical use for minor skin irritation relief. Storage instructions specify to store below 75°F (24°C). The label includes a barcode and notes Advanced Derm Solutions LLC as the trademark owner.*

FDA Label Image

Image Description (Label 30g 5)

The image shows the front label of Dermeleve soothing cream, a topical OTC product containing Aluminum Acetate at .2 g/100g strength. The label highlights its use for dry, itchy, and irritated skin, states it is steroid free, and lists additional ingredients such as strontium mineral salts, ceramides, hyaluronic acid, shea butter, and vitamins C and E. The net weight is 30g, and the product is made in the USA by Advanced Derm Solutions LLC.*

FDA Label Image

Image Description (Label 30g 6)

Drug Facts panel for Dermeleve cream containing Aluminum Acetate 0.2%, a topical astringent. It lists uses such as relief of minor skin irritations including poison ivy, poison oak, poison sumac, insect bites, athlete's foot, allergic itches, and minor burns. Warnings include external use only, avoid eyes, and not for open wounds. Directions cover use for adults and children two years and older. The panel also lists inactive ingredients and provides a manufacturer contact and website.*

FDA Label Image

Image Description (Label 3g 1)

Packaging label for Dermeleve Steroid Free Itch Relief Cream containing Aluminum Acetate at 0.2 g/100g strength in a 3g (0.1 oz) sachet. The label highlights the advanced formula with SrX-38® and states it is made in the USA. Labeler is Advanced Derm Solutions LLC.*

FDA Label Image

Image Description (Label 3g 2)

Drug Facts panel for Dermeleve cream containing Aluminum Acetate 0.2% as the active ingredient, labeled as an astringent. The panel lists uses such as chronic and severe itch, dry irritated skin, insect bites, allergic itch, and minor burns. It includes warnings, directions for use, and a detailed list of inactive ingredients. The label also shows the manufacturer Advanced Derm Solutions LLC, located in Ocala, FL, with contact information and a statement 'NOT FOR RESALE.'*

FDA Label Image

Image Description (Label 60g 1)

The front label of Dermeleve Soothing Cream features branding and highlights key product benefits such as relief for dry, itchy, and irritated skin. It lists active and notable ingredients including Aluminum Acetate 0.2%, Strontium Mineral Salts, Ceramides, Hyaluronic Acid, Shea Butter, and Vitamins C+E. The label notes the product is steroid-free, contains 60 grams, and is made in the USA by Advanced Derm Solutions LLC.*

FDA Label Image

Image Description (Label 60g 2)

Drug Facts panel for Dermeleve cream containing Aluminum Acetate 0.2% as the active ingredient with an astringent purpose. The panel lists uses for minor burns, insect bites, athlete's foot, and various rashes. It provides warnings for external use, eye contact, open wounds, and advises to stop use if condition worsens. Directions specify application for adults and children over two years. Inactive ingredients include water, shea butter, various emollients, and vitamins. The label is manufactured by Advanced Derm Solutions LLC.*

FDA Label Image

Image Description (Label 60g 3)

Label front of Dermeleve Soothing Cream with Aluminum Acetate 0.2% topical cream. The label highlights relief for dry, itchy, and irritated skin, steroid-free formulation, presence of SrX-38, and ingredients including strontium mineral salts, ceramides, hyaluronic acid, shea butter, and vitamins C and E. Package weight is 60 g and product is made in the USA by Advanced Derm Solutions LLC.*

FDA Label Image

Image Description (Label 60g 4)

Drug Facts panel for Dermeleve cream containing aluminum acetate 0.2%, labeled as an astringent. The panel lists uses including insect bites, minor burns, athlete's foot, and rashes. Warnings advise external use only, avoiding eyes, and not applying to open wounds. Directions specify use for adults and children over two years. Inactive ingredients and manufacturer Advanced Derm Solutions LLC are noted.*

FDA Label Image

Image Description (Label 60g 5)

Text panel for Dermeleve cream describing it as an advanced formula for dry and itchy skin. It highlights the SrX-38 proprietary formulation containing Aluminum Acetate and other soothing ingredients. The panel states the cream helps reduce irritation and lock in moisture for eczema-prone skin with regular use. It also notes the labeler as Advanced Derm Solutions LLC and the product weight as 60g.*

FDA Label Image

Image Description (Label 60g 6)

This image displays a partial drug information panel for Dermeleve Soothing Cream, a topical product containing aluminum acetate by Advanced Derm Solutions LLC. It states the cream is for all skin types and may be used for temporary relief of minor skin irritations. Storage instructions recommend keeping below 75°F (24°C). A barcode is also visible at the bottom.*

* 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.