SULFUR 8 MEDICATED DANDRUFF WITH SALICYLIC ACID- salicylic acid liquid

Country: United States

Language: English

Source: NLM (National Library of Medicine)

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Active ingredient:

SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ)

Available from:

J. Strickland and Co.

Administration route:

TOPICAL

Prescription type:

OTC DRUG

Therapeutic indications:

control the symptoms of  - dandruff  - seborrheic dermatitis - psoriasis

Authorization status:

OTC monograph final

Summary of Product characteristics

                                SULFUR 8 MEDICATED DANDRUFF WITH SALICYLIC ACID- SALICYLIC ACID LIQUID
J. STRICKLAND AND CO.
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SULFUR 8 MEDICATED DANDRUFF SHAMPOO WITH SALICYLIC ACID
_DRUG FACTS_
_ACTIVE INGREDIENT_
Salicylic Acid, 2%
_PURPOSE_
Antidandruff, Seborrheic dermatitis, Psoriasis.
_USES_
control the symptoms of
dandruff
seborrheic dermatitis
psoriasis
_WARNINGS_
FOR EXTERNAL USE ONLY
ASK A DOCTOR BEFORE USE
if you have
a condition that 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.
_DIRECTIONS_
For best results, use at least twice a week or as directed by a
doctor.
Apply a liberal amount of shampoo and massage into lather.
Allow lather to remain on scalp for a few minutes.
Rinse and repeat.
_INACTIVE INGRDIENTS_
Water, Sodium C14-16 Olefin Sulfonate, Cocamidopropyl Betaine, Sodium
Chloride,
Polyquaternium-22, Menthol, Aloe Barbadensis Leaf Extract, PEG-40
Hydrogenated
Castor Oil, Phenoxyethanol, Caprylyl Glycol, Ethylhexylglycerin,
Disodium EDTA, Sodium
Benzoate, Citric Acid, Potassium Sorbate, Sodium Sulfite, Sodium
Hydroxide, Benzyl
Benzoate, Fragrance.
PACKAGE LABELING:
SULFUR 8 MEDICATED DANDRUFF WITH SALICYLIC ACID
salicylic acid liquid
J. Strickland and Co.
PRODUCT INFORMATION
PRODUCT TYPE
HUMAN OTC DRUG
ITEM CODE (SOURCE)
NDC:12022-039
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)
SODIUM C14-16 OLEFIN SULFONATE (UNII: O9W3D3YF5U)
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
MENTHOL (UNII: L7T10EIP3A)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
POLYOXYL 40 HYDROGENATED 
                                
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