FDA.reportPublic FDA data

2.5OZ EverDry Antiperspirant Invisible

Manufacturer
American Consumer Products Corp
Effective date
2025-01-23
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
full-release
Hydrated at
2026-06-01 00:53:36

Label at a glance#

Product2.5OZ EverDry Antiperspirant Invisible
Active ingredientALUMINUM CHLOROHYDRATE
Label structure10 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredients: Aluminum Chlorohydrate 20%

OTC - PURPOSE SECTION

Purpose: Antiperspirant

WARNINGS SECTION

Warnings: For external use only.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, seek medical help or contact a Poison Control Center immediately.

INACTIVE INGREDIENT SECTION

Ingredients: Mineral Oil, Stearic Acid, Stearyl Alcohol, Zinc Palmitate, Cyclopentasiloxane, Hydrogenated Castor Oil, Fragrance, Silica, PPG-14 Butyl Ether, PEG-8 Disterate, BHT.

DOSAGE & ADMINISTRATION SECTION

Directions: Twist base. Smooth onto dry underarms. Apply to underarms only.

INSTRUCTIONS FOR USE SECTION

Use: reduces underarm wetness and perspiration.

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or rash develops.

INDICATIONS & USAGE SECTION

Do not use on broken or irritated skin.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

EverDry Anti PerspirantEverDry Anti Perspirant

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72197-017-022.5OZ EverDry Antiperspirant Invisible64 g in 1 TUBESTICK645

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
72197-0172.5OZ EVERDRY ANTIPERSPIRANT INVISIBLE (ALUMINUM CHLOROHYDRATE GEL) STICK [AMERICAN CONSUMER PRODUCTS CORP]5Current NDC, Legacy NDC, 1 package rows20250125_92c6ddc1-21cc-2164-e053-2a95a90a66cf.zip

Products#

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

DailyMed product names page 1 of 1 · 13 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72197-01772197-017-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 11 matching rows.

Name, UNII, Kind table
NameUNIIKind
ZINC PALMITATEQ7407964JAIACT
HYDROGENATED CASTOR OILZF94AP8MEYIACT
BUTYLATED HYDROXYTOLUENE1P9D0Z171KIACT
PPG-14 BUTYL ETHERR199TJT95TIACT
ALUMINUM CHLOROHYDRATEHPN8MZW13MACTIB
MINERAL OILT5L8T28FGPIACT
STEARIC ACID4ELV7Z65APIACT
STEARYL ALCOHOL2KR89I4H1YIACT
CYCLOMETHICONE 50THT5PCI0RIACT
SILICON DIOXIDEETJ7Z6XBU4IACT
PEG-8 DISTEARATE7JNC8VN07MIACT

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
2.5OZ EverDry Antiperspirant InvisibleALUMINUM CHLOROHYDRATE GELAmerican Consumer Products Corp92c6ddc1-21cc-2164-e053-2a95a90a66cf2025-01-23WarningsExact identifier
ndc (package): 72197-017-02
ndc (product): 72197-017
ndc11 (package): 72197001702
spl id: 2c69b385-9809-882c-e063-6294a90a7d37
spl set id: 92c6ddc1-21cc-2164-e053-2a95a90a66cf

Reported adverse events (FAERS/openFDA)#

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