ESIKA TOTAL SEC NEUTRAL FRAGRANCE ANTIPERSPIRANT AND DEODORANT UNISEX ROLL-ON ALL DAY EXTRA EFFECTIVE PROTECTION- aluminum sesquichlorohydrate emulsion

esika total sec NEUTRAL FRAGRANCE Antiperspirant and deodorant Unisex Roll-on All day extra effective protection by

Drug Labeling and Warnings

esika total sec NEUTRAL FRAGRANCE Antiperspirant and deodorant Unisex Roll-on All day extra effective protection by is a Otc medication manufactured, distributed, or labeled by BEL STAR S A. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Aluminum sesquichlorohydrate 15%

Purpose

Antiperspirant

Uses

Reduces underarm perspiration

WARNINGS

Warnings

For external use only

Do not use

on broken skin

Ask a doctor before use if you have

Kidney disease

Stop use 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, steareth-2, ppg-15 stearyl ether, cyclohexasiloxane, steareth-21, benzyl alcohol, dicaprylyl carbonate, 2-methyl 5-cyclohexylpentanol, bisabolol, hydroxyacetophenone, fragrance, tetrasodium edta, bht, propylene glycol, bambusa arundinacea leaf extract, potassium sorbate, sodium benzoate, hexyl cinnamal, limonene, linalool.

Product Packaging

total sec

NEUTRAL FRAGRANCE

Antiperspirant and deodorant

Unisex roll-on

All day extra effective protection

esika

1.6 fl. oz./50 ml

INGREDIENTS AND APPEARANCE

ESIKA TOTAL SEC NEUTRAL FRAGRANCE ANTIPERSPIRANT AND DEODORANT UNISEX ROLL-ON ALL DAY EXTRA EFFECTIVE PROTECTION 
aluminum sesquichlorohydrate emulsion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 14141-962
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALUMINUM SESQUICHLOROHYDRATE (UNII: UCN889409V) (ALUMINUM SESQUICHLOROHYDRATE - UNII:UCN889409V)	ALUMINUM SESQUICHLOROHYDRATE	15 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
PPG-15 STEARYL ETHER (UNII: 1II18XLS1L)
CYCLOMETHICONE 6 (UNII: XHK3U310BA)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
WATER (UNII: 059QF0KO0R)
2-METHYL 5-CYCLOHEXYLPENTANOL (UNII: 460837ILID)
HYDROXYACETOPHENONE (UNII: G1L3HT4CMH)
EDETATE SODIUM (UNII: MP1J8420LU)
STEARETH-21 (UNII: 53J3F32P58)
DICAPRYLYL CARBONATE (UNII: 609A3V1SUA)
LEVOMENOL (UNII: 24WE03BX2T)
BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
.ALPHA.-HEXYLCINNAMALDEHYDE (UNII: 7X6O37OK2I)
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
STEARETH-2 (UNII: V56DFE46J5)
BENZYL ALCOHOL (UNII: LKG8494WBH)
SODIUM BENZOATE (UNII: OJ245FE5EU)
LIMONENE, (+)- (UNII: GFD7C86Q1W)
LINALOOL, (+/-)- (UNII: D81QY6I88E)
BAMBUSA BAMBOS LEAF (UNII: HW86D1FGSS)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 14141-962-01	50 mL in 1 BOTTLE; Type 0: Not a Combination Product	06/07/2021

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M019	06/07/2021

Labeler - BEL STAR S A (880160197)

Establishment
Name	Address	ID/FEI	Business Operations
BEL STAR S A		880160197	manufacture(14141-962)