FDA.reportPublic FDA data

CYZONE NITRO DESODORANTE ANTITRANSPIRANTE ROLL ON

Manufacturer
BEL STAR SA
Effective date
2025-12-02
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:22:10

Label at a glance#

ProductCYZONE NITRO DESODORANTE ANTITRANSPIRANTE ROLL ON
Active ingredientALUMINUM SESQUICHLOROHYDRATE
Label structure7 sections

Label contents#

Full prescribing information#

Ingredientes activos

OTC - ACTIVE INGREDIENT SECTION

Aluminum sesquichlorohydrate 13.28%

Proposito

OTC - PURPOSE SECTION

Antitranspirante

Uso

INDICATIONS & USAGE SECTION

  • Reduce la transpiracion de las axilas.

Advertencias

WARNINGS SECTION

Solo para uso externo.

No usar

OTC - DO NOT USE SECTION

en piel danada o lastimada.

Consulte con el doctor

OTC - ASK DOCTOR SECTION

en caso de sufrir de enfermedad renal.

Detenga su uso si

OTC - STOP USE SECTION

sucede enrojecimiento.

Mantener fuera del alcance de los ninos.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Si es ingerido obtener ayuda medica o contactar al centro de Control de Envenenamiento inmediatamente.

Instrucciones

DOSAGE & ADMINISTRATION SECTION

  • Aplicar solamente en las axilas.

Ingredientes inactivos

INACTIVE INGREDIENT SECTION

water, steareth-2, ppg-15 stearyl ether, steareth-21, c13-15 alkane, fragrance, dicaprylyl carbonate, 2-methyl 5-cyclohexylpentanol, hydroxyacetophenone, tetrasodium edta, tetramethyl acetyloctahydronaphthalenes, hexamethylindanopyran, linalool, hexyl cinnamal, limonene, benzyl salicylate, linalyl acetate, acetyl cedrene, citrus limon (lemon) peel oil, citrus aurantium peel oil, coumarin, pinene, pogostemon cablin oil, citronellol, lavandula oil/extract, eugenol, citral, camphor, alpha-isomethyl ionone, beta-caryophyllene, vanillin, geraniol.

Package Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

11

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
14141-460-01CYZONE NITRO DESODORANTE ANTITRANSPIRANTE ROLL ON50 g in 1 BOTTLE, PLASTICEMULSION501

Products#

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

DailyMed product names page 1 of 1 · 33 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
14141-46014141-460-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 32 matching rows.

Name, UNII, Kind table
NameUNIIKind
GERANIOLL837108USYIACT
BETA-CARYOPHYLLENEBHW853AU9HIACT
HEXYL CINNAMAL7X6O37OK2IIACT
ALPHA-ISOMETHYL IONONE9XP4LC555BIACT
LINALOOLD81QY6I88EIACT
STEARETH-2V56DFE46J5IACT
TETRASODIUM EDTAMP1J8420LUIACT
LAVENDER OILZBP1YXW0H8IACT
DICAPRYLYL CARBONATE609A3V1SUAIACT
VANILLINCHI530446XIACT
CITRUS LIMON (LEMON) PEEL OILI9GRO824LLIACT
EUGENOL3T8H1794QWIACT
STEARETH-2153J3F32P58IACT
2-METHYL 5-CYCLOHEXYLPENTANOL460837ILIDIACT
ALUMINUM SESQUICHLOROHYDRATEUCN889409VACTIB
COUMARINA4VZ22K1WTIACT
LIMONENE, (+)-GFD7C86Q1WIACT
HYDROXYACETOPHENONEG1L3HT4CMHIACT
BENZYL SALICYLATEWAO5MNK9TUIACT
POGOSTEMON CABLIN OILF3IN55X5POIACT
WATER059QF0KO0RIACT
PPG-15 STEARYL ETHER1II18XLS1LIACT
C13-15 ALKANE114P5I43UJIACT
TETRAMETHYL ACETYLOCTAHYDRONAPHTHALENES2JU6ZH6GREIACT
HEXAMETHYLINDANOPYRAN14170060ATIACT
ACETYL CEDRENEX6I62755AKIACT
CITRONELLOLP01OUT964KIACT
PINENE996299PUKBIACT
LINALYL ACETATE5K47SSQ51GIACT
CITRUS AURANTIUM PEEL OIL9TLV70SV6IIACT
CITRALT7EU0O9VPPIACT
CAMPHOR (NATURAL)N20HL7Q941IACT

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
CYZONE NITRO DESODORANTE ANTITRANSPIRANTE ROLL ONALUMINUM SESQUICHLOROHYDRATEBEL STAR SA44fe14ab-d0b3-8e3d-e063-6394a90a0f742025-12-02WarningsExact identifier
ndc (package): 14141-460-01
ndc (product): 14141-460
ndc11 (package): 14141046001
spl id: 44fe178b-2a68-969d-e063-6394a90a4455
spl set id: 44fe14ab-d0b3-8e3d-e063-6394a90a0f74

Reported adverse events (FAERS/openFDA)#

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