FDA.reportPublic FDA data

Its you Antiperspirant Roll-on Deodorant

Manufacturer
Ventura Corporation LTD | BEL STAR S A
Effective date
2021-02-26
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 22:49:37

Label at a glance#

ProductIts you Antiperspirant Roll-on Deodorant
Active ingredientALUMINUM SESQUICHLOROHYDRATE
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient Purpose
Aluminum sesquichlorohydrate 13.60% Antiperspirant

OTC - PURPOSE SECTION

Uses

  • Reduces underarm perspiration

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.

INDICATIONS & USAGE SECTION

Stop use if rash or irritation occurs

WARNINGS SECTION

Warnings
For external use only
Do not use on broken skin
Ask a doctor before use if you have kidney disease

DOSAGE & ADMINISTRATION SECTION

Directions

  • Apply to underarms only.

INACTIVE INGREDIENT SECTION

Inactive ingredients: WATER, STEARETH-2, PPG-15 STEARYL ETHER, STEARETH-21, CYCLOHEXASILOXANE, FRAGRANCE, DICAPRYLYL CARBONATE, BENZYL ALCOHOL, 2-METHYL 5-CYCLOHEXYLPENTANOL, HYDROXYACETOPHENONE, TETRASODIUM EDTA, BISABOLOL, HEXYL CINNAMAL, LINALOOL, LIMONENE, BUTYLPHENYL METHYLPROPIONAL, CITRONELLOL, COUMARIN, GERANIOL, CITRAL.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

It's you

Antiperspirant roll-on Deodorant

esika

1.6 fl. oz. (50 ml)

Its you antiperspirantIts you antiperspirant

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
43596-0200-12025-04-22C16284748780-1f386c649-9bac-0266-e053-dadaa90a7c1aIt's you Antiperspirant Roll-on Deodorant
43596-0200-12023-01-30C16284748780-1f386c649-9bac-0266-e053-dadaa90a7c1aIt's you Antiperspirant Roll-on Deodorant

Products#

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

DailyMed product names page 1 of 1 · 20 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
43596-020043596-0200-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 19 matching rows.

Name, UNII, Kind table
NameUNIIKind
HYDROXYACETOPHENONEG1L3HT4CMHIACT
EDETATE SODIUMMP1J8420LUIACT
BENZYL ALCOHOLLKG8494WBHIACT
COUMARINA4VZ22K1WTIACT
GERANIOLL837108USYIACT
PPG-15 STEARYL ETHER1II18XLS1LIACT
.ALPHA.-HEXYLCINNAMALDEHYDE7X6O37OK2IIACT
STEARETH-2153J3F32P58IACT
STEARETH-2V56DFE46J5IACT
CYCLOMETHICONE 6XHK3U310BAIACT
DICAPRYLYL CARBONATE609A3V1SUAIACT
WATER059QF0KO0RIACT
ALUMINUM SESQUICHLOROHYDRATEUCN889409VACTIB
LIMONENE, (+)-GFD7C86Q1WIACT
CITRALT7EU0O9VPPIACT
.BETA.-CITRONELLOL, (R)-P01OUT964KIACT
BUTYLPHENYL METHYLPROPIONALT7540GJV69IACT
LEVOMENOL24WE03BX2TIACT
LINALOOL, (+)-F4VNO44C09IACT

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
3365cc64-47cb-513f-e063-6394a90af34dbc46db51-72c8-58e2-e053-2a95a90a07fd2025-04-22WarningsExact identifier
spl set id: bc46db51-72c8-58e2-e053-2a95a90a07fd

Reported adverse events (FAERS/openFDA)#

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