AARICA- aluminum chloride liquid

Aarica by

Drug Labeling and Warnings

Aarica by is a Otc medication manufactured, distributed, or labeled by The Podiatree Company. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

ACTIVE INGREDIENT

ALUMINUM CHLORIDE HEXAHYDRATE- 15%

PURPOSE

PURPOSE

ANTIPERSPIRANT

INDICATIONS & USAGE

USES

REDUCES EXCESSIVE PERSPIRATION AND WETNESS

WARNINGS

WARNING

For external use only.

DO NOT USE

DO NOT USE ON BROKEN SKIN

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

ASK DOCTOR

ASK A DOCTOR BEFORE USE IF YOU HAVE KIDNEY DISEASE.

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

QUESTIONS

QUESTIONS OR SUGGESTIONS? 1.855.763.8733 or visit us at www.thepodiatreecompany.com

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

AARICA 
aluminum chloride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 54633-413
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALUMINUM CHLORIDE (UNII: 3CYT62D3GA) (ALUMINUM CATION - UNII:3XHB1D032B)	ALUMINUM CHLORIDE	15 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
CAMELLIA SINENSIS WHOLE (UNII: C5M4585ZBZ)
HYDROXYETHYL CELLULOSE (100 MPA.S AT 2%) (UNII: R33S7TK2EP)
POLYSORBATE 80 (UNII: 6OZP39ZG8H)
ALCOHOL (UNII: 3K9958V90M)
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 54633-413-03	88.72 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/06/2014

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part350	05/06/2014

Labeler - The Podiatree Company (078656000)