Zero sweat 20% Lotion

Manufacturer: I Shay Cosmetics Inc.
Effective date: 2021-06-23
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 23:41:03

Label at a glance#

ProductZero Sweat

Active ingredientALUMINUM SESQUICHLOROHYDRATE

Label structure8 sections

Indications and uses

Uses treats excessive perspiration

Label contents#

Full prescribing information#

dosage & administration

DOSAGE & ADMINISTRATION SECTION

Directions

wash and dry area thoroughly before application

apply a small amount

rub in vigorously for a minimum of 15 seconds

allow time to dry

inactive ingredients

INACTIVE INGREDIENT SECTION

water

propylene glycol

isopropyl myristate

glycol stearate

cetearyl alcohol

polysorbate 60

aluminum starch octenlysuccinate

dmethicone

butyl hydroxyl toluene

indications and usage

INDICATIONS & USAGE SECTION

Uses

treats excessive perspiration

active ingredient

OTC - ACTIVE INGREDIENT SECTION

aluminum sesquichlorohydrate

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

warnings

for externasl use only

do not use on irritated skin

stop use and ask doctor is rash or irritation develops

ask a doctor before use if you have kidney disease

label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

label

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
65112-267-01	2024-01-30	C162847	48780-1	1030e365-10cd-111a-e063-dadaa90a10e2	Zero sweat 20% Lotion

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
65112-267-01	Zero Sweat	47.9 g in 1 TUBE	LOTION	47.9		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
65112-267	ZERO SWEAT (ZERO SWEAT LOTION) LOTION [I SHAY COSMETICS INC.]	1	Legacy NDC, 1 package rows	20210627_c5752af2-6d76-0a3d-e053-2995a90ad542.zip

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

Zero Sweat
Zero sweat Lotion
ALUMINUM SESQUICHLOROHYDRATE
GLYCOL STEARATE
PROPYLENE GLYCOL
ISOPROPYL MYRISTATE
WATER

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
65112-267	65112-267-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
ALUMINUM SESQUICHLOROHYDRATE	UCN889409V	ACTIB
GLYCOL STEARATE	0324G66D0E	IACT
PROPYLENE GLYCOL	6DC9Q167V3	IACT
ISOPROPYL MYRISTATE	0RE8K4LNJS	IACT
WATER	059QF0KO0R	IACT

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
c5752af2-6d77-0a3d-e053-2995a90ad542			c5752af2-6d76-0a3d-e053-2995a90ad542	2021-06-23	Warnings	Exact identifier spl id: c5752af2-6d77-0a3d-e053-2995a90ad542 spl set id: c5752af2-6d76-0a3d-e053-2995a90ad542

Reported adverse events (FAERS/openFDA)#

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