FDA.reportPublic FDA data

ALUMINUM SESQUICHLOROHYDRATE

Manufacturer
Bel Star S.A. (Colombia)
Effective date
2019-11-15
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 00:00:58

Label at a glance#

ProductESIKA TOTAL SEC NEUTRAL FRAGRANCE ANTIPERSPIRANT AND DEODORANT ALL DAY EXTRA EFFECTIVE PROTECTION
Active ingredientALUMINUM SESQUICHLOROHYDRATE
Label structure9 sections

Indications and uses

Reduces underarm perspiration

Dosage and administration

Apply to underarms only.

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Aluminum sesquichlorohydrate 16.00%

Purpose

OTC - PURPOSE SECTION

Antiperspirant

Uses

INDICATIONS & USAGE SECTION

  • Reduces underarm perspiration

Warnings

WARNINGS SECTION

For external use only

OTC - DO NOT USE SECTION

Do not use on broken skin

OTC - ASK DOCTOR SECTION

Ask a doctor before use if you have Kidney desease

OTC - STOP USE SECTION

Stop use and ask a doctor if rash or irritation occurs

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

WATER, STEARETH-2, STEARETH-21, PPG-15 STEARYL ETHER, CYCLOPENTASILOXANE, CYCLOHEXASILOXANE, DICAPRYLYL CARBONATE, BISABOLOL, TRICLOSAN, METHYLPARABEN, FRAGRANCE, BENZALKONIUM CHLORIDE, BHT, PROPYLENE GLYCOL, TETRASODIUM EDTA, BAMBUSA ARUNDINACEA LEAF EXTRACT, HEXYL CINNAMAL, d-LIMONENE, LINALOOL.

SPL UNCLASSIFIED SECTION

Dist. by Ventura Corp, Ltd., San Juan, Puerto Rico
00926.

PRINCIPAL DISPLAY PANEL - 50 ml Bottle Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

ésika
total
sec

NEUTRAL FRAGRANCE

Antiperspirant
and deodorant
Alcohol – free
Unisex Roll-on
All day extra
effective protection

36

50 ml e (1.7 fl.oz.)

PRINCIPAL DISPLAY PANEL - 50 ml Bottle Label
PRINCIPAL DISPLAY PANEL - 50 ml Bottle Label

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
14141-96414141-964-01

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
ALUMINUM SESQUICHLOROHYDRATEUCN889409VACTIB
WATER059QF0KO0RIACT
STEARETH-2V56DFE46J5IACT
STEARETH-2153J3F32P58IACT
PPG-15 STEARYL ETHER1II18XLS1LIACT
CYCLOMETHICONE 50THT5PCI0RIACT
CYCLOMETHICONE 6XHK3U310BAIACT
DICAPRYLYL CARBONATE609A3V1SUAIACT
LEVOMENOL24WE03BX2TIACT
TRICLOSAN4NM5039Y5XIACT
METHYLPARABENA2I8C7HI9TIACT
BENZALKONIUM CHLORIDEF5UM2KM3W7IACT
BUTYLATED HYDROXYTOLUENE1P9D0Z171KIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
EDETATE SODIUMMP1J8420LUIACT
BAMBUSA BAMBOS LEAFHW86D1FGSSIACT
.ALPHA.-HEXYLCINNAMALDEHYDE7X6O37OK2IIACT
LIMONENE, (+)-GFD7C86Q1WIACT
LINALOOL, (+/-)-D81QY6I88EIACT

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
0cd489c3-034e-0156-e063-6294a90a31c13911df73-2ad4-47e4-996e-60de2e4d58042023-12-18WarningsExact identifier
spl set id: 3911df73-2ad4-47e4-996e-60de2e4d5804

Reported adverse events (FAERS/openFDA)#

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