ESIKA PULSO CHRISTIAN MEIER ANTIPERSPIRANT ROLL-ON DEODORANT FM

Manufacturer
Ventura Corporation LTD | Bel Star S.A. (Colombia)
Effective date
2015-12-28
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 01:29:27

Label at a glance#

ProductESIKA PULSO CHRISTIAN MEIER ANTIPERSPIRANT ROLL-ON DEODORANT FM
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 13.60 %

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, ppg-15 stearyl ether, steareth-21, fragrance, dicaprylyl carbonate, cyclopentasiloxane, benzyl alcohol, triclosan, cyclohexasiloxane, hydroxyacetophenone, tetrasodium edta, bisabolol.

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

pulso
CHRISTIAN MEIER

ANTIPERSPIRANT
ROLL-ON DEODORANT FM
dose not contain alcohol

ésika

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#

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
13537-72813537-728-01

Ingredients#

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

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

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
312d66db-dd69-b586-e063-6394a90af0dd598b3194-40cd-4643-ad81-fb4cd72db4792025-03-25WarningsExact identifier
spl set id: 598b3194-40cd-4643-ad81-fb4cd72db479

Reported adverse events (FAERS/openFDA)#

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