FDA.reportPublic FDA data

Pulso Absolute Antiperspirant Roll-on Deodorant

Manufacturer
Ventura Corporation Limited | Bel Star S.A. (Colombia)
Effective date
2021-03-03
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 22:49:33

Label at a glance#

ProductPulso Absolute 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, COUMARIN, ALPHA-ISOMETHYL IONONE, GERANIOL, CITRAL, CITRONELLOL.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Pulso Absolute

Antiperspirant Roll-on Deodorant

esika

1.6 fl.oz. (50ml)

Pulso Antiperspirant 1Pulso Antiperspirant 1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
43596-0201-12025-04-22C16284748780-1f386c649-ce7b-0266-e053-dadaa90a7c1aPulso Absolute Antiperspirant Roll-on Deodorant
43596-0201-12023-01-30C16284748780-1f386c649-ce7b-0266-e053-dadaa90a7c1aPulso Absolute Antiperspirant Roll-on Deodorant

Products#

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

DailyMed product names page 1 of 1 · 19 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
43596-020143596-0201-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 18 matching rows.

Name, UNII, Kind table
NameUNIIKind
GERANIOLL837108USYIACT
CITRALT7EU0O9VPPIACT
.BETA.-CITRONELLOL, (R)-P01OUT964KIACT
STEARETH-2153J3F32P58IACT
STEARETH-2V56DFE46J5IACT
ALUMINUM SESQUICHLOROHYDRATEUCN889409VACTIB
CYCLOMETHICONE 6XHK3U310BAIACT
HYDROXYACETOPHENONEG1L3HT4CMHIACT
EDETATE SODIUMMP1J8420LUIACT
LEVOMENOL24WE03BX2TIACT
COUMARINA4VZ22K1WTIACT
PPG-15 STEARYL ETHER1II18XLS1LIACT
LIMONENE, (+)-GFD7C86Q1WIACT
DICAPRYLYL CARBONATE609A3V1SUAIACT
ISOMETHYL-.ALPHA.-IONONE9XP4LC555BIACT
BENZYL ALCOHOLLKG8494WBHIACT
WATER059QF0KO0RIACT
LINALOOL, (+/-)-D81QY6I88EIACT

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
3365d7ad-31e0-5138-e063-6394a90af2efbca9f45a-70bf-2c9e-e053-2a95a90a2eb42025-04-22WarningsExact identifier
spl set id: bca9f45a-70bf-2c9e-e053-2a95a90a2eb4

Reported adverse events (FAERS/openFDA)#

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