Zero Sweat

Manufacturer: I Shay Cosmetics Inc
Effective date: 2021-06-18
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: legacy-cache
Hydrated at: 2026-08-01 22:42:48

Label at a glance#

ProductZero Sweat

Active ingredientALUMINUM CHLORIDE

Label structure10 sections

Indications and uses

Uses Decreases excessive perspiration Decreases underarm sweating

Dosage and administration

Directions Apply to underarms Apply sparingly Apply only at bedtime Apply only a few strokes under each arm

Label contents#

Full prescribing information#

Active

OTC - ACTIVE INGREDIENT SECTION

Aluminum Chloride 15% antiperspriant

ASk Doctor

OTC - ASK DOCTOR SECTION

Ask a doctor before use if you have kidney disease.

Keep out of reach of children

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.

Purpose

OTC - PURPOSE SECTION

antiperspirant

Warnings

WARNINGS SECTION

For external use only

Do not Use: immediately after shaving; on irritated skin; on broken skin; immediately after bathing

When Using

OTC - WHEN USING SECTION

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

Dosage and Administration

DOSAGE & ADMINISTRATION SECTION

Directions

Apply to underarms

Apply sparingly

Apply only at bedtime

Apply only a few strokes under each arm

Inactive Ingredients

INACTIVE INGREDIENT SECTION

water, sodium bicarbonate

Indications and usage

INDICATIONS & USAGE SECTION

Uses

Decreases excessive perspiration

Decreases underarm sweating

Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

Zero Sweat
Zero Sweat 15%
WATER
SODIUM BICARBONATE
ALUMINUM CHLORIDE
ALUMINUM CATION

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
65112-266	65112-266-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
WATER	059QF0KO0R	IACT
SODIUM BICARBONATE	8MDF5V39QO	IACT
ALUMINUM CHLORIDE	3CYT62D3GA	ACTIB

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
dbd908d6-f62a-04d7-e053-2a95a90aef64			c510b16b-9a1f-199f-e053-2995a90a67d1	2022-04-04	Warnings	Exact identifier spl set id: c510b16b-9a1f-199f-e053-2995a90a67d1

Reported adverse events (FAERS/openFDA)#

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