Sulfur 8 Original Anti-dandruff Hair And Scalp Conditioner Ointment
Product Images NDC 12022-017

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Sulfur 8 Original Anti-dandruff Hair And Scalp Conditioner (NDC 12022-017). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by J. Strickland & Co., 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

017 00

Label for Sulfur 8 medicated Original Formula anti-dandruff hair and scalp conditioner ointment containing 2% sulfur as the active ingredient. The net weight is 2 oz (57g). Manufactured by J. Strickland & Co., the label includes drug facts, directions for use, warnings, inactive ingredients, and a barcode. The product is topical and controls scalp itching and flaking due to dandruff.*

FDA Label Image

017 01

Label for Sulfur 8 Original Anti-Dandruff Hair and Scalp Conditioner ointment, medicated with sulfur 2%. The yellow label includes the brand name Sulfur 8 and states it is an anti-dandruff hair and scalp conditioner with a net weight of 4 oz (113 g). Manufacturer is J. Strickland & Co. Additional text includes drug facts, active ingredient, warnings, directions, and a list of inactive ingredients.*

FDA Label Image

017 02

Label for Sulfur 8 Original Anti-Dandruff Hair and Scalp Conditioner ointment, medicated formula. The label states 2% sulfur as the active ingredient for anti-dandruff use. The product net weight is 7.25 oz (205 g). It is labeled by J. Strickland & Co., with a reorder number 432-1. The label includes Drug Facts and a barcode on a yellow background.*

* 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.