Glovers Dandruff Control Medicine, Regular Suspension
FDA Label NDC 12022-007

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 Dandruff Control Medicine, Regular (NDC 12022-007). 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, 2.5%

Purpose

Antidandruff

Uses:

Controls scalp itching and flaking due to dandruff

Warnings:

For External Use Only.

When Using This Product

  • do not get into eyes. If contact occurs rinse eyes thoroughly with water.

Stop Use And Consult A Doctor If

  • if skin irritation develops or increases.
  • 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 at once.

Directions:

  • Shake well before using.
  • For best results, use at leats twice a week, or as directed  by a doctor.
  • Before shampooimg your hair, apply a small amount to the scalp in several areas. Rub in well. Wait 15 minutes to 1 hour Shampoo thoroughly

Inactive Ingredients:

Mineral Oil (Paraffum Liquidum), Polysorbate-85, Disteardimonium Hectorite, Propylene Glycol, Benzyl Alcohol, Fragrance (Parfum).

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