GLOVERS DANDRUFF CONTROL MED., FLORAL- sulfur suspension

Glovers Dandruff Control Med., Floral by

Drug Labeling and Warnings

Glovers Dandruff Control Med., Floral by is a Otc medication manufactured, distributed, or labeled by J. Strickland & Co.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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​

Package Labeling Carton

INGREDIENTS AND APPEARANCE

GLOVERS DANDRUFF CONTROL MED., FLORAL 
sulfur suspension

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 12022-008
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SULFUR (UNII: 70FD1KFU70) (SULFUR - UNII:70FD1KFU70)	SULFUR	25 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
MINERAL OIL (UNII: T5L8T28FGP)
POLYSORBATE 85 (UNII: A7F3N56197)
DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
BENZYL ALCOHOL (UNII: LKG8494WBH)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 12022-008-00	1 in 1 CARTON	11/05/2001
1		81 mL in 1 BOTTLE; Type 0: Not a Combination Product

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	Business Operations
J. Strickland & Co.		007023112	manufacture(12022-008) , pack(12022-008) , label(12022-008)