GLOVERS MEDICATED ANTI-DANDRUFF SCALP- salicylic acid solution

Glovers Medicated Anti-Dandruff Scalp by

Drug Labeling and Warnings

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

Drug Details [pdf]

Active Ingredient

Salicylic Acid, 3%

Purposes

Antidandruff,

Seborrheic Dermatitis,

Psoriasis

Use

for relief of scalp itching, irritation, redness, scaling and flaking associated with dandruff, seborrheic dermatitis and psoriasis.

Warnings:

For External Use Only.

Ask a doctor before use if

the condition covers a large area of the body

When using this product

• avoid contact with eyes. If contact occurs, rinse eyes thoroughly with water.

Stop use and ask a doctor if

condition worsens or does not improve after regular use of this product as directed.

Keep out of reach of children

If swallowed, get medical help or call a poison control center right away.

Flammable

Keep away from heat and open flame.

Directions:

• Apply to the affected area one to four times daily or as directed by a doctor
• Use after shampooing or between shampoos.

Inactive Ingredients:

SD Alcohol 40, Water, Propylene Glycol, Benzyl Alcohol, Menthol.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

GLOVERS MEDICATED ANTI-DANDRUFF SCALP 
salicylic acid solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 12022-011
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ)	SALICYLIC ACID	30 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
BENZYL ALCOHOL (UNII: LKG8494WBH)
MENTHOL (UNII: L7T10EIP3A)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 12022-011-00	1 in 1 CARTON	11/05/2001
1		75 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(12022-011) , pack(12022-011) , label(12022-011)