GLOVERS ANTI-DANDRUFF- sulfur, salicylic acid ointment

Glovers Anti-Dandruff by

Drug Labeling and Warnings

Glovers 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

Sulfur, 5%

Salicylic Acid, 3%

Purpose

Antidandruff

Antidandruff

Uses

• relieves the itching and scaling associated with dandruff

Warnings

For external use only

When using this product

• Do not get in eyes. If contact occurs, rinse eyes thoroughly with water

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

Apply a small amount to the scalp one to four times daily or as directed by a doctor

Inactive Ingredients

Petrolatum, Mineral Oil, Glyceryl Tribehenate, Arachidyl Propionate, Fragrance, Polysorbate-20, Propylparaben, Iron Oxides, Talc.

Package Labeling 12022-009-00

Package Labeling 12022-009-01

INGREDIENTS AND APPEARANCE

GLOVERS ANTI-DANDRUFF 
sulfur, salicylic acid ointment

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 12022-009
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SULFUR (UNII: 70FD1KFU70) (SULFUR - UNII:70FD1KFU70)	SULFUR	50 mg  in 1 g
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ)	SALICYLIC ACID	30 mg  in 1 g

Inactive Ingredients
Ingredient Name	Strength
PETROLATUM (UNII: 4T6H12BN9U)
MINERAL OIL (UNII: T5L8T28FGP)
TRIBEHENIN (UNII: 8OC9U7TQZ0)
ARACHIDYL PROPIONATE (UNII: QV5DAH3MSB)
POLYSORBATE 20 (UNII: 7T1F30V5YH)
PROPYLPARABEN (UNII: Z8IX2SC1OH)
FERRIC OXIDE RED (UNII: 1K09F3G675)
TALC (UNII: 7SEV7J4R1U)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 12022-009-00	28 g in 1 JAR; Type 0: Not a Combination Product	09/20/2001
2	NDC: 12022-009-01	99 g in 1 JAR; Type 0: Not a Combination Product	09/20/2001

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part358H	09/20/2001

Labeler - J. Strickland & Co. (007023112)

Registrant - J. Strickland & Co. (007023112)

Establishment
Name	Address	ID/FEI	Business Operations
J. Strickland & Co.		007023112	manufacture(12022-009) , pack(12022-009) , label(12022-009)