Dr. Johne Skin Tag Remover Solution
Product Images NDC 85818-001

Product Visual Gallery

This gallery contains 8 technical images submitted to the FDA as part of the official labeling for Dr. Johne Skin Tag Remover (NDC 85818-001). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Dr.johnes 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

Package1 Of 10 mL (Img1 10ml)

Packaging label for Dr. Johne SKIN TAG REMOVER topical solution containing Salicylic Acid 17%. The label includes the brand name, product name, usage for removal of skin tags, common warts, corns, and calluses, and a net volume of 10 mL. It also shows the labeler as Dr.Johnes LLC with a barcode and usage directions on the side panel.*

FDA Label Image

Package1 Of 7 mL (Img1 7ml)

Dr. Johne SKIN TAG REMOVER topical solution, 7 mL, contains Salicylic Acid 17% as the active ingredient. The dark blue packaging features the brand name and product purpose, with an image of a skin tag. The label includes drug facts, warnings, directions, inactive ingredients, and manufacturer information: Dr. Johnes LLC, Sheridan, Wyoming. It also displays a barcode and disposal icons.*

FDA Label Image

Package1 Of 8 mL (Img1 8ml)

Dr. Johne SKIN TAG REMOVER packaging label for a topical solution containing 170 mg/mL Salicylic Acid. The label shows the brand name, product name, a net volume of 8 mL, and manufacturer Dr.Johnes LLC. The label includes drug facts, directions, warnings, uses, and inactive ingredients. It also features images depicting skin tag removal results, a barcode, and recycling and disposal icons.*

FDA Label Image

Package1 Of 9 mL (Img1 9ml)

Dr. Johne SKIN TAG REMOVER topical solution containing Salicylic Acid 17% is presented in a 9 ml package by Dr. Johnes LLC. The carton is predominantly dark blue with white text and includes drug facts, usage instructions, warnings, inactive ingredients, and contact information. It features images showing its use for removing skin tags and similar skin issues. The label also includes a barcode and recycling symbols.*

FDA Label Image

Package2 Of 10 mL (Img2 10ml)

Label for Dr. Johne SKIN TAG REMOVER topical solution containing 17% salicylic acid as the active ingredient. The label highlights its use as a wart, corn, and callus remover. It includes inactive ingredients such as menthol and various plant extracts. Directions advise cleaning and drying the affected area and applying a thin layer once or twice daily, with warnings against use on open wounds or infected skin. The net volume is 10 mL.*

FDA Label Image

Package2 Of 7 mL (Img2 7ml)

Label for Dr. Johne SKIN TAG REMOVER topical solution, containing 17% Salicylic Acid as the active ingredient. The label highlights its purpose as a wart, corn, and callus remover and lists inactive ingredients including menthol, Coptis chinensis extract, and ethanol. Net volume is 7 mL. Directions advise cleaning the affected area, applying a thin layer once or twice daily, and avoiding use on open wounds or infected skin.*

FDA Label Image

Package2 Of 8 mL (Img2 8ml)

Dr. Johne SKIN TAG REMOVER topical solution with 17% salicylic acid, for wart, corn, and callus removal. The label includes inactive ingredients like menthol and botanical extracts. Directions advise cleaning the affected area and applying a thin layer once or twice daily, avoiding open wounds. Net volume is 8 mL, labeler Dr.Johnes LLC.*

FDA Label Image

Package2 Of 9 mL (Img2 9ml)

Label for Dr. Johne SKIN TAG REMOVER topical solution containing 17% salicylic acid, used as a wart, corn, and callus remover. The label lists inactive ingredients including menthol, Coptis chinensis extract, and others, with directions for application. The net volume is 9 ml. Labeled by Dr.Johnes 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.