FDA.reportPublic FDA data

Aarica

Manufacturer
The Podiatree Company
Effective date
2017-12-19
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-05-31 22:53:33

Label at a glance#

ProductAarica
Active ingredientALUMINUM CHLORIDE
Label structure13 sections

Storage and handling

OTHER INFORMATION STORE AT CONTROLLED ROOM TEMPERATURE.

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

ACTIVE INGREDIENT

ALUMINUM CHLORIDE HEXAHYDRATE- 15%

OTC - PURPOSE SECTION

PURPOSE

ANTIPERSPIRANT

INDICATIONS & USAGE SECTION

USES

REDUCES EXCESSIVE PERSPIRATION AND WETNESS

WARNINGS SECTION

WARNING

For external use only.

OTC - DO NOT USE SECTION

DO NOT USE ON BROKEN SKIN

OTC - STOP USE SECTION

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 SECTION

ASK A DOCTOR BEFORE USE IF YOU HAVE KIDNEY DISEASE.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

DOSAGE & ADMINISTRATION SECTION

DIRECTIONS

APPLY EVENLY AT BEDTIME OR AS DIRECTED BY YOUR DOCTOR.

STORAGE AND HANDLING SECTION

OTHER INFORMATION

STORE AT CONTROLLED ROOM TEMPERATURE.

INACTIVE INGREDIENT SECTION

INACTIVE INGREDIENTS: CAMELLIA SINENSIS (BLACK TEA) LEAF EXTRACT, FRAGRANCE, HYDROXYETHYL CELLULOSE, POLYSORBATE 80, SD 40 ALCOHOL (20%), SODIUM BICARBONATE, WATER

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

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DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
fb7ab793-2c12-4079-b100-a64f73bef25aProduct name420240712
b0cbf770-6cc3-4aa4-9158-755110c2b9f7Product name220230717
dc7c5daa-021f-40dd-b00d-63982cb2067aProduct name120230426
08ffbcbf-26df-b99c-1dab-64fc4cfae89fProduct name520200925
816b97af-edc5-4060-aff1-b814bdbcad50Product name120190415
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
419aab54-5d5a-4146-9453-026d4a9991beProduct name220170525
08ffbcbf-26df-b99c-1dab-64fc4cfae89fProduct name220160823
89dac932-b90a-4410-9ab1-84c53e57de25Product name120150316

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
54633-413-03Aarica88.72 mL in 1 BOTTLELIQUID88.723

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
54633-413AARICA (ALUMINUM CHLORIDE) LIQUID [THE PODIATREE COMPANY]3Legacy NDC, 1 package rows20171220_60b9862e-04ec-2b6a-e053-2a91aa0ab8e5.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
54633-41354633-413-03

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
NameUNIIKind
CAMELLIA SINENSIS WHOLEC5M4585ZBZIACT
HYDROXYETHYL CELLULOSE (100 MPA.S AT 2%)R33S7TK2EPIACT
POLYSORBATE 806OZP39ZG8HIACT
ALCOHOL3K9958V90MIACT
SODIUM BICARBONATE8MDF5V39QOIACT
WATER059QF0KO0RIACT
ALUMINUM CHLORIDE3CYT62D3GAACTIB

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
60b91648-c805-7468-e053-2991aa0a6c1e60b9862e-04ec-2b6a-e053-2a91aa0ab8e52017-12-19WarningsExact identifier
spl id: 60b91648-c805-7468-e053-2991aa0a6c1e
spl set id: 60b9862e-04ec-2b6a-e053-2a91aa0ab8e5

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.