FDA.reportPublic FDA data

ESIKA

Manufacturer
Ventura Corporation LTD. | Bel Star S.A. (Colombia)
Effective date
2011-12-16
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 01:50:01

Label at a glance#

ProductESIKA EXPRESSION Roll-on
Active ingredientAluminum Sesquichlorohydrate
Label structure9 sections

Indications and uses

reduces underarm wetness.

Dosage and administration

apply to underarms only.

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Aluminum sesquichlorohydrate (17%)

Purpose

OTC - PURPOSE SECTION

Antiperspirant

Uses

INDICATIONS & USAGE SECTION

  • reduces underarm wetness.

Warnings

WARNINGS SECTION

  • For external use only.

OTC - DO NOT USE SECTION

  • Do not use on broken skin.

OTC - STOP USE SECTION

  • Stop use and ask a doctor if rash and irritation occurs.

OTC - ASK DOCTOR SECTION

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

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.

Directions

DOSAGE & ADMINISTRATION SECTION

  • apply to underarms only.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Aqua (water), ppg-15 stearyl ether, steareth-2, steareth-21, fragrance, dicaprylyl carbonate, cyclopentasiloxane, triclosan, cyclohexasiloxane, benzalkonium chloride, tetrasodium edta, methylparaben, bisabolol.

SPL UNCLASSIFIED SECTION

PR: Distributed by Ventura Corporation, Ltd. San Juan, Puerto Rico 00926.

PRINCIPAL DISPLAY PANEL - 50 ml Bottle Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Expression

ANTIPERSPIRANT
ROLL-ON DEODORANT
does not contain alcohol

ēsika

50 ml e (1.7 fl.oz.)

Principal Display Panel - 50 ml Bottle Label
Principal Display Panel - 50 ml Bottle Label

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
13537-423-012025-04-24C16284748780-197449f38-d016-f6ea-e053-dbdaa90aa703Expression ANTIPERSPIRANT ROLL-ON DEODORANT
13537-423-012019-11-13C16284748780-197449f38-d016-f6ea-e053-dbdaa90aa703Expression ANTIPERSPIRANT ROLL-ON DEODORANT

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
Aluminum SesquichlorohydrateACTIVE INGREDIENTUCN889409V1
Aluminum SesquichlorohydrateACTIVE MOIETYUCN889409V1

Products#

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

DailyMed product names page 1 of 1 · 13 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
13537-42313537-423-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 12 matching rows.

Name, UNII, Kind table
NameUNIIKind
Aluminum SesquichlorohydrateUCN889409VACTIB
water059QF0KO0RIACT
steareth-2V56DFE46J5IACT
steareth-2153J3F32P58IACT
dicaprylyl carbonate609A3V1SUAIACT
cyclomethicone 50THT5PCI0RIACT
triclosan4NM5039Y5XIACT
cyclomethicone 6XHK3U310BAIACT
benzalkonium chlorideF5UM2KM3W7IACT
edetate sodiumMP1J8420LUIACT
methylparabenA2I8C7HI9TIACT
levomenol24WE03BX2TIACT

Source Document#

Source XML · Source PDF

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
338ac573-bad4-3925-e063-6394a90a65e991933a55-4921-4f1d-8620-8b99ea2eadf52025-04-24WarningsExact identifier
spl set id: 91933a55-4921-4f1d-8620-8b99ea2eadf5

Reported adverse events (FAERS/openFDA)#

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