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ESIKA EXPRESSION ANTIPERSPIRANT ROLL-ON DEODORANT

Medically reviewed on July 13, 2018

Dosage form: emulsion
Ingredients: ALUMINUM SESQUICHLOROHYDRATE 0.136g in 1mL
Labeler: Ventura Corporation LTD
NDC Code: 13537-961

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

ÉSIKA EXPRESSION ANTIPERSPIRANT ROLL-ON DEODORANT

Drug Facts

Active Ingredient

Aluminum sesquichlorohydrate 13.60%

Purpose

Antiperspirant

Uses
  • Reduces underarm perspiration

Warnings

For external use only

Do not use on broken skin

Ask a doctor before use if you have Kidney desease

Stop use and ask a doctor if rash or irritation occurs

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

Directions
  • Apply to underarms only.

Inactive ingredients

WATER, PPG-15 STEARYL ETHER, STEARETH-2, STEARETH-21, FRAGRANCE, DICAPRYLYL CARBONATE, CYCLOPENTASILOXANE, TRICLOSAN, CYCLOHEXASILOXANE, METHYLPARABEN, TETRASODIUM EDTA, BENZALKONIUM CHLORIDE, BISABOLOL, BUTYLPHENYL METHYLPROPIONAL, AMYL CINNAMAL, LINALOOL, HEXYL CINNAMAL, CITRONELLOL, BENZYL SALICYLATE, BENZYL BENZOATE, CINNAMYL ALCOHOL, d-LIMONENE, GERANIOL, HYDROXYCITRONELLAL, ALPHA-ISOMETHYL IONONE, EUGENOL.

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

PRINCIPAL DISPLAY PANEL - 50 ml Bottle Label

Expression

ANTIPERSPIRANT
ROLL-ON DEODORANT
does not contain alcohol

ésika

50 ml e (1.7 fl.oz.)

ESIKA EXPRESSION ANTIPERSPIRANT ROLL-ON DEODORANT 
aluminum sesquichlorohydrate emulsion
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:13537-961
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALUMINUM SESQUICHLOROHYDRATE (ALUMINUM SESQUICHLOROHYDRATE) ALUMINUM SESQUICHLOROHYDRATE0.136 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER 
PPG-15 STEARYL ETHER 
STEARETH-2 
STEARETH-21 
DICAPRYLYL CARBONATE 
CYCLOMETHICONE 5 
TRICLOSAN 
CYCLOMETHICONE 6 
METHYLPARABEN 
EDETATE SODIUM 
BENZALKONIUM CHLORIDE 
LEVOMENOL 
BUTYLPHENYL METHYLPROPIONAL 
.ALPHA.-AMYLCINNAMALDEHYDE 
LINALOOL, (+/-)- 
.ALPHA.-HEXYLCINNAMALDEHYDE 
.BETA.-CITRONELLOL, (R)- 
BENZYL SALICYLATE 
BENZYL BENZOATE 
CINNAMYL ALCOHOL 
LIMONENE, (+)- 
GERANIOL 
HYDROXYCITRONELLAL 
ISOMETHYL-.ALPHA.-IONONE 
EUGENOL 
Packaging
#Item CodePackage Description
1NDC:13537-961-0150 mL in 1 BOTTLE, PLASTIC
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH FINALpart35007/08/2016
Labeler - Ventura Corporation LTD (602751344)
Establishment
NameAddressID/FEIOperations
Bel Star S.A. (Colombia)880160197MANUFACTURE(13537-961)

 
Ventura Corporation LTD

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Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.

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