FDA.reportPublic FDA data

Sure Unscented Antiperspirant and Deodorant

Manufacturer
Sodalis USA LLC
Effective date
2024-11-08
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 00:35:33

Label at a glance#

ProductSure Unscented Antiperspirant and Deodorant
Active ingredientALUMINUM CHLOROHYDRATE ANHYDROUS
Label structure7 sections

Dosage and administration

apply to underarms only shake well before each use 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 120ºF

Do not use

OTC - DO NOT USE SECTION

on broken skin

Ask a doctor before use if you have

OTC - ASK DOCTOR/PHARMACIST SECTION

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

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

Directions

DOSAGE & ADMINISTRATION SECTION

  • apply to underarms only
  • shake well before each use
  • hold can about 6 inches away from underarm and spray.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Butane, Hydrofluorocarbon 152a, Cyclopentasiloxane, Aluminum Chlorohydrate, Isopropyl Palmitate, Dimethicone, Disteardimonium Hectorite, Propylene Carbonate, Ethylene Brassylate.

Package Labelling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
81277-007-01Sure Unscented Antiperspirant and Deodorant170 g in 1 CANAEROSOL, SPRAY1702

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
81277-007SURE UNSCENTED ANTIPERSPIRANT AND DEODORANT (ALUMINUM CHLOROHYDRATE ANHYDROUS) AEROSOL, SPRAY [SODALIS USA LLC]2Current NDC, 1 package rows20241109_3a3aac47-7a03-4efe-a6df-724081cd02c0.zip

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
81277-00781277-007-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

Name, UNII, Kind table
NameUNIIKind
BUTANE6LV4FOR43RIACT
1,1-DIFLUOROETHANE0B1U8K2ME0IACT
CYCLOMETHICONE 50THT5PCI0RIACT
ISOPROPYL PALMITATE8CRQ2TH63MIACT
DIMETHICONE92RU3N3Y1OIACT
DISTEARDIMONIUM HECTORITEX687XDK09LIACT
PROPYLENE CARBONATE8D08K3S51EIACT
ETHYLENE BRASSYLATE9A87HC7RODIACT
ALUMINUM CHLOROHYDRATE ANHYDROUS407PSC3OC7ACTIB

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 Unscented Antiperspirant and DeodorantALUMINUM CHLOROHYDRATE ANHYDROUSSodalis USA LLC3a3aac47-7a03-4efe-a6df-724081cd02c02024-11-08WarningsExact identifier
ndc (package): 81277-007-01
ndc (product): 81277-007
ndc11 (package): 81277000701
spl id: 266b9490-4cc0-a0ee-e063-6294a90a44a6
spl set id: 3a3aac47-7a03-4efe-a6df-724081cd02c0

Reported adverse events (FAERS/openFDA)#

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