Otc - Active Ingredient
ACTIVE INGREDIENT
ALUMINUM CHLORIDE HEXAHYDRATE- 15%
Aarica
FDA Label NDC 54633-413
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by The Podiatree Company for the product Aarica (NDC 54633-413). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding otc - active ingredient, otc - purpose, indications & usage, warnings, otc - do not use, otc - stop use, otc - ask doctor, otc - keep out of reach of children, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
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
* Please review the disclaimer below.
