Glovers Anti-dandruff Ointment
FDA Label NDC 12022-009

Full FDA labeling including Indications, Dosage, Usage, and Precautions

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by J. Strickland & Co. for the product Glovers Anti-dandruff (NDC 12022-009). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.

This specific version of the label includes detailed information regarding active ingredients, purpose, uses, warnings, when using this product, stop use and consult a doctor if, keep out of reach of children, directions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Active Ingredients

Sulfur, 5%

Salicylic Acid, 3%

Purpose

Antidandruff

Antidandruff

Uses

  • relieves the itching and scaling associated with dandruff

Warnings

For external use only

When Using This Product

  • Do not get in eyes. If contact occurs, rinse eyes thoroughly with water

Stop Use And Consult A Doctor If

  • condition worsens or does not improve after regular use.

Keep Out Of Reach Of Children

If swallowed, get medical help or call a Poison Control Center right away.

Directions

Apply a small amount to the scalp one to four times daily or as directed by a doctor

Inactive Ingredients

Petrolatum, Mineral Oil, Glyceryl Tribehenate, Arachidyl Propionate, Fragrance, Polysorbate-20, Propylparaben, Iron Oxides, Talc.

Package Labeling

* Please review the disclaimer below.