FDA.reportPublic FDA data

Sure Complete Confidence Antiperspirant Deodorant Aerosol, Unscented

Manufacturer
Sodalis USA, LLC
Effective date
2025-02-18
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 00:55:27

Label at a glance#

ProductSure Complete Confidence Antiperspirant Deodorant Aerosol, Unscented
Active ingredientALUMINUM CHLOROHYDRATE
Label structure7 sections

Dosage and administration

• apply to underarms only • hold can about 6 inches away from underarm and spray.

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Aluminum Chlorohydrate 10% (anhydrous)

Purpose

OTC - PURPOSE SECTION

Antiperspirant

Use

INDICATIONS & USAGE SECTION

reduces underarm wetness

Warnings

WARNINGS SECTION

For external use only.

Flammable

• do not spray near flame or while smoking
• contents under pressure
• do not crush, puncture or incinerate
• do not store at temperature above 120°F

Do not use

OTC - DO NOT USE SECTION

on broken skin

Ask a doctor before use

OTC - ASK DOCTOR SECTION

if you have kidney disease

When using this product

OTC - WHEN USING SECTION

• keep away from face and mouth to avoid breathing it
• avoid spraying in eyes
• use only as directed; intentional misuse by deliberately concentrating and inhaling the contents can be harmful or fatal

Stop use if

OTC - STOP USE SECTION

rash or irritation occurs

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

lf swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

• apply to underarms only
• hold can about 6 inches away from underarm and spray.

Inactive ingredients:

INACTIVE INGREDIENT SECTION

Isobutane, Cyclopentasiloxane, Hydrofluorocarbon 152 A, Propane, Dimethicone, Propylene Carbonate, Disteardimonium Hectorite, Butane, Ethylene Brassylate.

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Outer Package2Outer Package2Inner Package2Inner Package2

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
81277-011-01Sure Complete Confidence Antiperspirant Deodorant Aerosol, Unscented170 g in 1 CANAEROSOL, SPRAY1701

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
81277-011SURE COMPLETE CONFIDENCE ANTIPERSPIRANT DEODORANT AEROSOL, UNSCENTED (ALUMINUM CHLOROHYDRATE) AEROSOL, SPRAY [SODALIS USA, LLC]1Current NDC, 1 package rows20250221_000a4912-a633-46b4-9aff-725fdeeef7c0.zip

Products#

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

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
81277-01181277-011-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 matching rows.

Name, UNII, Kind table
NameUNIIKind
ISOBUTANEBXR49TP611IACT
CYCLOPENTASILOXANE0THT5PCI0RIACT
1,1-DIFLUOROETHANE0B1U8K2ME0IACT
PROPANET75W9911L6IACT
DIMETHICONE92RU3N3Y1OIACT
PROPYLENE CARBONATE8D08K3S51EIACT
DISTEARDIMONIUM HECTORITEX687XDK09LIACT
BUTANE6LV4FOR43RIACT
ETHYLENE BRASSYLATE9A87HC7RODIACT
ALUMINUM CHLOROHYDRATEHPN8MZW13MACTIB

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
Sure Complete Confidence Antiperspirant Deodorant Aerosol, UnscentedALUMINUM CHLOROHYDRATESodalis USA, LLC000a4912-a633-46b4-9aff-725fdeeef7c02025-02-18WarningsExact identifier
ndc (package): 81277-011-01
ndc (product): 81277-011
ndc11 (package): 81277001101
spl id: 2e70f4b3-7b97-af33-e063-6294a90a1186
spl set id: 000a4912-a633-46b4-9aff-725fdeeef7c0

Reported adverse events (FAERS/openFDA)#

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