SULFUR 8 SCALP THERAPY MEDICATED DANDRUFF CONTROL- salicylic acid spray

Sulfur 8 Scalp Therapy Medicated Dandruff Control by

Drug Labeling and Warnings

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

Drug Details [pdf]

Drug Facts

Active Ingredient

Salicylic Acid, 2%

Purpose

Antidandruff

Use:

Controls scalp itching and flaking due to dandruff

Warnings

For external use only

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 call a Poison Control Center at once.

Directions

Spray to apply to the affected area 1-4 times daily, or as directed by a doctor

Inactive Ingredients

Water, Glycerin, Sodium Hydroxide, PEG-40 Hydrogenate Castor Oil, PEG-12 Dimethicone, Propylene Glycol, Hydrolyzed Collagen, Diazolidinyl Urea, Disodium EDT, Methylparaben, Propylparaben, Ethylhexylglycerin, PEG-12 Alyl Ether, PEG-12, Butylene Glycol, Phenoxyethanol, Fragrance

Package Labeling:

INGREDIENTS AND APPEARANCE

SULFUR 8 SCALP THERAPY MEDICATED DANDRUFF CONTROL 
salicylic acid spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 12022-032
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ)	SALICYLIC ACID	20 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
PEG-12 DIMETHICONE (300 CST) (UNII: ZEL54N6W95)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)
EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)
METHYLPARABEN (UNII: A2I8C7HI9T)
PROPYLPARABEN (UNII: Z8IX2SC1OH)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
POLYETHYLENE GLYCOL 600 (UNII: NL4J9F21N9)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
PHENOXYETHANOL (UNII: HIE492ZZ3T)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 12022-032-00	355 mL in 1 BOTTLE; Type 0: Not a Combination Product	01/01/2020

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)