FDA.reportPublic FDA data

Pulso Antiperspirant Roll-on Deodorant

Manufacturer
Bel Star S.A. (Colombia)
Effective date
2022-12-08
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 21:45:05

Label at a glance#

ProductPulso Antiperspirant Roll-on Deodorant
Active ingredientALUMINUM SESQUICHLOROHYDRATE
Label structure9 sections

Indications and uses

Reduces underarm perspiration

Dosage and administration

Apply to underarms only

Label contents#

Full prescribing information#

Active ingredient purpose

OTC - ACTIVE INGREDIENT SECTION

ALUMINUM SESQUICHLOROHYDRATE 13.60 %

Uses

OTC - PURPOSE SECTION

Reduces underarm perspiration

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

INDICATIONS & USAGE SECTION

Stop use if rash or irritation occurs

Warnings

WARNINGS SECTION

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

DOSAGE & ADMINISTRATION SECTION

Apply to underarms only

INACTIVE INGREDIENT SECTION

Water, Steareth-2, PPG-15 Stearyl Ether, Steareth-21, Fragrance, Dicaprylyl Carbonate, Cyclopentasiloxane, Benzyl Alcohol, Triclosan, Cyclohexasiloxane, Hydroxyacetophenone, Tetrasodium EDTA, Bisabolol, Linalool, d-limonene, Coumarin, Alpha-Isomethyl Ionone, Citral, Geraniol, Citronellol

SPL UNCLASSIFIED SECTION

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

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Pulso

Antiperspirant Roll-on deodorant

esika

50ml e (1.6 fl. oz.)

Pulso roll onPulso roll on

Products#

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

DailyMed product names page 1 of 1 · 21 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
14141-05014141-050-01

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
EDETATE SODIUMMP1J8420LUIACT
COUMARINA4VZ22K1WTIACT
GERANIOLL837108USYIACT
WATER059QF0KO0RIACT
LEVOMENOL24WE03BX2TIACT
HYDROXYACETOPHENONEG1L3HT4CMHIACT
CITRALT7EU0O9VPPIACT
.BETA.-CITRONELLOL, (R)-P01OUT964KIACT
PPG-15 STEARYL ETHER1II18XLS1LIACT
STEARETH-2153J3F32P58IACT
CYCLOMETHICONE 50THT5PCI0RIACT
LINALOOL, (+/-)-D81QY6I88EIACT
LIMONENE, (+)-GFD7C86Q1WIACT
DICAPRYLYL CARBONATE609A3V1SUAIACT
BENZYL ALCOHOLLKG8494WBHIACT
TRICLOSAN4NM5039Y5XIACT
CYCLOMETHICONE 6XHK3U310BAIACT
ISOMETHYL-.ALPHA.-IONONE9XP4LC555BIACT
ALUMINUM SESQUICHLOROHYDRATEUCN889409VACTIB

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
ef54ee1f-0c96-503e-e053-2995a90a310099623b6b-1a97-24e3-e053-2995a90a4dbe2022-12-08WarningsExact identifier
spl id: ef54ee1f-0c96-503e-e053-2995a90a3100
spl set id: 99623b6b-1a97-24e3-e053-2995a90a4dbe

Reported adverse events (FAERS/openFDA)#

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