Glovers Dandruff Control Med., Floral: Package Insert and Label Information

GLOVERS DANDRUFF CONTROL MED., FLORAL- sulfur suspension
J. Strickland & Co.

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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.

Flammable

Keep away from heat and open flame

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).

​Package Labeling Bottle

Bottle
(click image for full-size original)

Package Labeling Carton

Carton
(click image for full-size original)

GLOVERS DANDRUFF CONTROL MED., FLORAL
sulfur suspension
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:12022-008
Route of Administration TOPICAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
SULFUR (SULFUR) SULFUR 25 mg in 1 mL
Inactive Ingredients
Ingredient Name Strength
MINERAL OIL
POLYSORBATE 85
DISTEARDIMONIUM HECTORITE
PROPYLENE GLYCOL
BENZYL ALCOHOL
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:12022-008-00 1 BOTTLE in 1 CARTON contains a BOTTLE
1 81 mL in 1 BOTTLE This package is contained within the CARTON (12022-008-00)
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC monograph final part358H 11/05/2001
Labeler — J. Strickland & Co. (007023112)
Registrant — J. Strickland & Co. (007023112)
Establishment
Name Address ID/FEI Operations
J. Strickland & Co. 007023112 manufacture (12022-008), pack (12022-008), label (12022-008)

Revised: 11/2019 J. Strickland & Co.

DrugInserts.com provides trustworthy package insert and label information about marketed drugs as submitted by manufacturers to the US Food and Drug Administration. Package information is not reviewed or updated separately by DrugInserts.com. Every individual package label entry contains a unique identifier which can be used to secure further details directly from the US National Institutes of Health and/or the FDA.

As the leading independent provider of trustworthy medication information, we source our database directly from the FDA's central repository of drug labels and package inserts under the Structured Product Labeling standard. Our material is not intended as a substitute for direct consultation with a qualified health professional.

Terms of Use | Copyright © 2019. All Rights Reserved.