Glovers Anti-dandruff Ointment
Product Images NDC 12022-009

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Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Glovers Anti-dandruff (NDC 12022-009). 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.

Product Images & Figures Index

FDA Label Image

12022 009 00 1

12022 009 00 1
Glover's Imperial Medicated Ointment is a topical treatment for dandruff associated with scaling and itching. The ointment contains 5% sulfur and salicylic acid. It is for external use only and should be applied to the affected area up to four times a day or as directed by a doctor. The product warns to avoid contact with eyes and to rinse thoroughly with water if contact occurs. It also recommends stopping use and consulting a doctor if the condition worsens or does not improve. The ointment comes in a 1 oz (28g) container and contains other inactive ingredients like Petrolatum, Mineral Oil, and Propylparaben. This product is manufactured by J. Strickland & Co. in Olive Branch, MS.*
FDA Label Image

12022 009 01 2

12022 009 01 2
Glover's Imperial Medicated Ointment is a drug used to relieve the itching and scaling linked with dandruff. It is to be applied to the scalp as directed and is made in the USA. The ointment contains active anti-dandruff ingredients as well as inactive ingredients such as petrolatum, mineral oil, and talc. It is not advised to get the product in your eyes, and if any adverse effects are experienced, you should seek medical attention.*

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