FDA.reportPublic FDA data

KIWI ANTIPERSPIRANT DEODORANT ROLL-ON

Manufacturer
Evi Labs
Effective date
2026-01-08
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 01:31:55

Label at a glance#

ProductKIWI ANTIPERSPIRANT DEODORANT ROLL-ON
Active ingredientALUMINUM CHLOROHYDRATE
Label structure10 sections

Dosage and administration

SHAKE WELL BEFORE USE. APPLY TO UNDERARMS ONLY CLOSE TIGHT AFTER USE.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

kiwi from renderkiwi from renderActive Ingredient: Aluminum chlorohydrate 10%.

kiwi back renderkiwi back render

Purpose

OTC - PURPOSE SECTION

Antiperspirant

Use

USE IN SPECIFIC POPULATIONS SECTION

Reduces underarm perspiration

Warnings

WARNINGS SECTION

For external use only

Do not use on broken skin

Stop use if rash or irritation occurs

Ask a doctor before use if you have a kidney disease.

Keep of reach of children. If swallowed, get medical help or contact a Poison Control Center night away.

INSTRUCTIONS FOR USE SECTION

Shake well before use. Apply to underarms only. Close tight after use.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Fragrance, Poly aminopropyl Biguanide, PPG-15 Stearyl Ether, Steareth-2, Steareth-21, Water, Glycerin/ Actinidia Chinensis Fruit Extract/Sodium Benzoate/ Potassium Sorbate ( Fruit Ectract).

INDICATIONS & USAGE

INDICATIONS & USAGE SECTION

Do not use on broken skin.

Stop use if rash or irritation occurs.

DIRECTIONS

DOSAGE & ADMINISTRATION SECTION

SHAKE WELL BEFORE USE. APPLY TO UNDERARMS ONLY CLOSE TIGHT AFTER USE.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep of reach of children. If swallowed, get medical help or contact

Poison Control Center night away.

Package Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Kiwi PanelKiwi Panel

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130431407451742GTIN-13: 0431407451742
EAN-13: 0431407451742
GTIN-12: 431407451742
UPC-A: 431407451742
GTIN storage (14 digits): 00431407451742		kiwi panel.jpg, kiwi back render.jpg

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
84178-009-03KIWI ANTIPERSPIRANT DEODORANT ROLL-ON80 g in 1 BOTTLE, PLASTICCREAM803

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
84178-00984178-009-03

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
NameUNIIKind
PPG-15 STEARYL ETHER1II18XLS1LIACT
STEARETH-2V56DFE46J5IACT
STEARETH-2153J3F32P58IACT
ALUMINUM CHLOROHYDRATEHPN8MZW13MACTIB
POLYAMINOPROPYL BIGUANIDEDT9D8Z79ETIACT
WATER059QF0KO0RIACT

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
KIWI ANTIPERSPIRANT DEODORANT ROLL-ONANTIPERSPIRANT DEODORANT ROLL-ONEvi Labs15371589-7581-4690-e063-6294a90a6ca12026-01-08WarningsExact identifier
ndc (package): 84178-009-03
ndc (product): 84178-009
ndc11 (package): 84178000903
spl id: 47e248b3-5c6f-8131-e063-6394a90a9d8e
spl set id: 15371589-7581-4690-e063-6294a90a6ca1

Reported adverse events (FAERS/openFDA)#

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