SULFUR 8 SCALP THERAPY MEDICATED DANDRUFF CONTROL LEAVE-IN SOOTHING TREATMENT- salicylic acid solution

Sulfur 8 Scalp Therapy Medicated Dandruff Control Leave-In Soothing Treatment by

Drug Labeling and Warnings

Sulfur 8 Scalp Therapy Medicated Dandruff Control Leave-In Soothing Treatment by is a Otc medication manufactured, distributed, or labeled by J. Strickland and Co.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Salicylic Acid, 2%

Purpose

Antidandruff, Seborrheic Dermatitis, Psoriasis

Use:

for relief of scalp itching, irritation, redness, scaling and flaking associated with dandruff, seborrheic dermatitis, 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, rinse eyes thoroughly with water.

Stop use and consult 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 contact 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

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

Package Labeling:

INGREDIENTS AND APPEARANCE

SULFUR 8 SCALP THERAPY MEDICATED DANDRUFF CONTROL LEAVE-IN SOOTHING TREATMENT 
salicylic acid solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 12022-033
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: 12022-033-00	1 in 1 BOX	01/01/2020
1		74 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	01/01/2020

Labeler - J. Strickland and Co. (007023112)