ZeroSweat Antiperspirant 12%

Manufacturer
I. Shay Cosmetics
Effective date
2024-11-13
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 00:37:05

Label at a glance#

ProductZeroSweat Antiperspirant 12%
Active ingredientALUMINUM CHLORIDE
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Aluminum Chloride- 12%

OTC - PURPOSE SECTION

Antiperspirant

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

WARNING: Keep out of reach of children

INDICATIONS & USAGE SECTION

Decreases excessive perspiration.

Decreases underarm sweating.

INACTIVE INGREDIENT SECTION

Purified Water, Aloe Vera Extract, Allantoin, Willow Bark Extract, Chamomile Extract, Glycerin, Sodium Bicarbonate.

WARNINGS SECTION

For External Use Only.

Ask a doctor before use if you have kidney disease.

Do not use:

-Immediately after shaving

-On irritated skin

-On broken skin

-Immediately after bathing

When using this product do not use in or near eyes.

Stop use and ask doctor if rash or irritation develops

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

DOSAGE & ADMINISTRATION SECTION

Apply to appropriate body area. Apply sparingly. Apply only a few strokes under each arm. Apply only at bedtime.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Zero Sweat antiperspirantZero Sweat antiperspirant

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
65112-306-01ZeroSweat Antiperspirant 12%35.5 mL in 1 BOTTLE, WITH APPLICATORLOTION35.51
65112-306-02ZeroSweat Antiperspirant 12%1 in 1 BOXLOTION11

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
65112-306ZEROSWEAT ANTIPERSPIRANT 12% (ANTIPERSPIRANT) LOTION [I. SHAY COSMETICS]12 package rows20241115_26d6548b-5513-9bc5-e063-6394a90aee4a.zip

Products#

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

DailyMed product names page 1 of 1 · 5 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
65112-30665112-306-01, 65112-306-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
NameUNIIKind
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
26d6548b-5514-9bc5-e063-6394a90aee4a26d6548b-5513-9bc5-e063-6394a90aee4a2024-11-13WarningsExact identifier
spl id: 26d6548b-5514-9bc5-e063-6394a90aee4a
spl set id: 26d6548b-5513-9bc5-e063-6394a90aee4a

Reported adverse events (FAERS/openFDA)#

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