GLOVERS MEDICATED ANTI-DANDRUFF- coal tar shampoo

Glovers Medicated Anti-Dandruff by

Drug Labeling and Warnings

Glovers Medicated Anti-Dandruff by is a Otc medication manufactured, distributed, or labeled by J. Strickland & Co.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredients

Coal Tar Solution, 2.5%

Purpose

Antidandruff, Antipsoriasis (Equivalent to Coal Tar USP, 0.5%)

Uses:

Controls scalp itching and flaking due to dandruff

Warnings:

For external use only

Ask A doctor before use

• if the condition covers a large area of your body
• with other forms of psoriasis therapy such as prescription drugs or UV radition

When using this product

• Do not get into eyse. If contact occurs, rinse eyes thoroughly with water
• Use caution in exposing the skin to sunlight after using this product. It may increase your tendency to sunburn for up to 24 hours after application.

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

• Wet hair, apply to scalp and massage. Rinse and repeat.
• For best results, use at least twice a week.

Inactive Ingredients

Water, Ammonium Lauryl Sulfate, Ammonium Laureth Sufate, Polysorbate-20, Potassiuym Cocoyl Hydrolyzed Collagen, Cocamidopropyl Betaine, PEG-3 Glyceryl Cocoate, Fragrance, Benzyl Alcohol, Methylchloroisothiazolinone, Methylisothiazolinone, Triethylene Glycol, Propylene Glycol, Magnesium Nitrate, Magnesium Chloride, Citric Acid.

Package Labeling

INGREDIENTS AND APPEARANCE

GLOVERS MEDICATED ANTI-DANDRUFF 
coal tar shampoo

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 12022-010
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
COAL TAR (UNII: R533ESO2EC) (COAL TAR - UNII:R533ESO2EC)	COAL TAR	25 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
AMMONIUM LAURYL SULFATE (UNII: Q7AO2R1M0B)
POLYSORBATE 20 (UNII: 7T1F30V5YH)
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
BENZYL ALCOHOL (UNII: LKG8494WBH)
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
TRIETHYLENE GLYCOL (UNII: 3P5SU53360)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
MAGNESIUM NITRATE (UNII: 77CBG3UN78)
MAGNESIUM CHLORIDE (UNII: 02F3473H9O)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 12022-010-00	118 mL in 1 BOTTLE; Type 0: Not a Combination Product	10/31/2001

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part358H	10/31/2001

Labeler - J. Strickland & Co. (007023112)

Registrant - J. Strickland & Co. (007023112)

Establishment
Name	Address	ID/FEI	Business Operations
J. Strickland & Co.		007023112	manufacture(12022-010) , pack(12022-010) , label(12022-010)