FDA Label for Renewal Anti-dandruff
View Indications, Usage & Precautions
Renewal Anti-dandruff Product Label
The following document was submitted to the FDA by the labeler of this product Rite Aid Corporation. 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.
Active Ingredient
SALICYLIC ACID 2%
Purpose
ANTI-DANDRUFF/ ANTI-SEBORRHEIC DERMATITIS/ ANTI-PSORIASIS
Uses
CONTROLS THE SYMPTOMS OF DANDRUFF, SEBORRHEIC DERMATITIS, AND 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
- FOR USE ON COLOR TREATED OR PERMED HAIR, RINSE THOROUGHLY
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
IN CASE OF ACCIDENTAL INGESTION, GET MEDICAL HELP OR CONTACT A POISON CONTROL CENTER IMMEDIATELY
Directions
- FOR BEST RESULTS, USE TWICE A WEEK OR AS DIRECTED BY A DOCTOR
- WET HAIR, MASSAGE ONTO SCALP FOR SEVERAL MINUTES, AND THEN RINSE
- REPEAT IF DESIRED
Inactive Ingredients
WATER (AQUA), SODIUM LAURETH SULFATE, ACRYLATES CROSSPOLYMER-4, COCAMIDE MEA, SODIUM COCOYL SARCOSINATE, GLYCOL DISTEARATE, POLYQUATERNIUM-7, FRARANCE (PARFUM), SODIUM CHLORIDE, SODIUM HYDROXIDE, TETRASODIUM EDTA, BHT, METHYLCHLOROISOTHIAZOLINONE, METHYLISOTHIAZOLINONE, BLUE 1 (CI 42090)
Questions Or Comments?
1-866-695-3030
Label Copy
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