FDA Label for Head And Shoulders Clinical Moisturizing Scalp
View Indications, Usage & Precautions
Head And Shoulders Clinical Moisturizing Scalp Product Label
The following document was submitted to the FDA by the labeler of this product The Procter & Gamble Manufacturing Company. The document includes published materials associated whith this product with the essential scientific information about this product as well as other prescribing information. Product labels may durg indications and usage, generic names, contraindications, active ingredients, strength dosage, routes of administration, appearance, warnings, inactive ingredients, etc.
Other
Drug Facts
Dist. by PROCTER & GAMBLE,
CINCINNATI, OH 45202
Active Ingredient
Pyrithione zinc .2%
Purpose
Anti-dandruff
Uses
helps prevent recurrence of flaking and itching associated with dandruff.
Otc - Do Not Use
For external use only.
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.
Otc - Keep Out Of Reach Of Children
Keep this and all drugs out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
Directions
- apply to affected areas one to four times daily or as directed by a doctor.
Inactive Ingredients
Water, stearyl alcohol, cetyl alcohol, stearamidopropyl dimethylamine, glutamic acid, phenoxyethanol, benzyl alcohol, fragrance, methylparaben, dimethicone, propylparaben, citric acid, honey extract.
Questions (Or Comments)?
1-800-723-9569
Principal Display Panel - 125 Ml Bottle
head &
shoulders
®
pyrithione zinc dandruff treatment
CLINICAL
MOISTURIZING
SCALP CREAM
HYDRATES DRY SCALP
USE BETWEEN WASHES
W I T H MA N U KA HONE Y
4.2 FL OZ (125 mL)
* Please review the disclaimer below.