ZeroSweat with Aloe

Manufacturer
I Shay Cosmetics Inc
Effective date
2024-11-13
Label type
HUMAN OTC DRUG LABEL
Version
12
Source
full-release
Hydrated at
2026-06-01 00:37:10

Label at a glance#

ProductZeroSweat with Aloe
Active ingredientALUMINUM CHLORIDE
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Aluminum Chloride 12% ... Antiperspirant

OTC - PURPOSE SECTION

Antiperspirant

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

WARNING: Keep out of reach of children.

INDICATIONS & USAGE SECTION

Reduces underarm perspiration.

INACTIVE INGREDIENT SECTION

Purified Water, Glycerin (Skin Emollient), Allantoin, Chamomile Flower Extract, Aloe Barbadensis Leaf Juice, Salix Alba “Willow” Bark Extract (Botanical Extract Blend), Sodium Bicarbonate.

WARNINGS SECTION

For external use only.

Do not use:

  • Immediately after shaving
  • Immediately after bathing
  • On irritated skin
  • On broken skin

Stop use if rash occurs
Ask a doctor before use if you have kidney disease

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

DOSAGE & ADMINISTRATION SECTION

Apply to the appropriate body area.

Apply only at bedtime

Apply sparingly

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
65112-259-012024-11-13C16284748780-11030e365-5d39-111a-e063-dadaa90a10e2ZeroSweat Antiperspirant 12%
65112-259-012024-01-30C16284748780-11030e365-5d39-111a-e063-dadaa90a10e2ZeroSweat Antiperspirant 12%

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
65112-259-01ZeroSweat with Aloe28.35 g in 1 BOTTLE, GLASSLIQUID28.3512

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
65112-259ZEROSWEAT WITH ALOE (ANTIPERSPIRANT) LIQUID [I SHAY COSMETICS INC]12Legacy NDC, 1 package rows20241115_92ddc7b0-d8a6-0783-e053-2995a90a03e9.zip

Products#

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

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

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
65112-25965112-259-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

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
26d25fc6-4d32-43d5-e063-6394a90a25dd92ddc7b0-d8a6-0783-e053-2995a90a03e92024-11-13WarningsExact identifier
spl id: 26d25fc6-4d32-43d5-e063-6394a90a25dd
spl set id: 92ddc7b0-d8a6-0783-e053-2995a90a03e9

Reported adverse events (FAERS/openFDA)#

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