FDA.reportPublic FDA data

Esika Winner Sport Antiperspirant Roll-on Deodorant

Manufacturer
Ventura Corporation LTD | Bel Star S.A. (Colombia)
Effective date
2020-10-23
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:10:09

Label at a glance#

ProductEsika Winner Sport 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, linalool, limonene, hexyl cinnamal, butylphenyl methylpropional, benzyl salicylate, isoeugenol, coumarin, citral, geraniol, benzyl alcohol, citronellol

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Esika Winner Sport Antiperspirant Roll-on Deodorant

1.6 fl. oz. (50ml)

ET 56844 AET 56844 A

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
43596-0099-12025-04-07C16284748780-1d6a99b39-fe92-a426-e053-dadaa90af4c2Esika Winner Sport Antiperspirant Roll-on Deodorant
43596-0099-12022-01-28C16284748780-1d6a99b39-fe92-a426-e053-dadaa90af4c2Esika Winner Sport Antiperspirant Roll-on Deodorant

Products#

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

DailyMed product names page 1 of 1 · 23 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
43596-009943596-0099-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 22 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALUMINUM SESQUICHLOROHYDRATEUCN889409VACTIB
STEARETH-2V56DFE46J5IACT
BENZYL ALCOHOLLKG8494WBHIACT
.BETA.-CITRONELLOL, (R)-P01OUT964KIACT
CITRALT7EU0O9VPPIACT
LIMONENE, (+)-GFD7C86Q1WIACT
.ALPHA.-HEXYLCINNAMALDEHYDE7X6O37OK2IIACT
BUTYLPHENYL METHYLPROPIONALT7540GJV69IACT
GERANIOLL837108USYIACT
BENZYL SALICYLATEWAO5MNK9TUIACT
ISOEUGENOL5M0MWY797UIACT
COUMARINA4VZ22K1WTIACT
2-METHYL 5-CYCLOHEXYLPENTANOL460837ILIDIACT
DICAPRYLYL CARBONATE609A3V1SUAIACT
CYCLOMETHICONE 6XHK3U310BAIACT
PPG-15 STEARYL ETHER1II18XLS1LIACT
STEARETH-2153J3F32P58IACT
LINALOOL, (+)-F4VNO44C09IACT
WATER059QF0KO0RIACT
HYDROXYACETOPHENONEG1L3HT4CMHIACT
EDETATE SODIUMMP1J8420LUIACT
LEVOMENOL24WE03BX2TIACT

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
323968de-89a1-9e7d-e063-6394a90af57eb258eaa8-5b86-e8c5-e053-2995a90aafb52025-04-07WarningsExact identifier
spl set id: b258eaa8-5b86-e8c5-e053-2995a90aafb5

Reported adverse events (FAERS/openFDA)#

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