FDA Label for Aarica
View Indications, Usage & Precautions
Aarica Product Label
The following document was submitted to the FDA by the labeler of this product The Podiatree 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.
Otc - Active Ingredient
ACTIVE INGREDIENT
ALUMINUM CHLORIDE HEXAHYDRATE- 15%
Otc - Purpose
PURPOSE
ANTIPERSPIRANT
Indications & Usage
USES
REDUCES EXCESSIVE PERSPIRATION AND WETNESS
Warnings
WARNING
For external use only.
Otc - Do Not Use
DO NOT USE ON BROKEN SKIN
Otc - Stop Use
STOP USE AND ASK A DOCTOR OR PHARMACIST IF SKIN IRRITATION OR SENSITIVITY DEVELOPS OR INCREASES OR IF THE CONDITION PERSISTS OR GETS WORSE
Otc - Ask Doctor
ASK A DOCTOR BEFORE USE IF YOU HAVE KIDNEY DISEASE.
Otc - Keep Out Of Reach Of Children
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
Dosage & Administration
DIRECTIONS
APPLY EVENLY AT BEDTIME OR AS DIRECTED BY YOUR DOCTOR.
Storage And Handling
OTHER INFORMATION
STORE AT CONTROLLED ROOM TEMPERATURE.
Inactive Ingredient
INACTIVE INGREDIENTS: CAMELLIA SINENSIS (BLACK TEA) LEAF EXTRACT, FRAGRANCE, HYDROXYETHYL CELLULOSE, POLYSORBATE 80, SD 40 ALCOHOL (20%), SODIUM BICARBONATE, WATER
Otc - Questions
QUESTIONS OR SUGGESTIONS? 1.855.763.8733 or visit us at www.thepodiatreecompany.com
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