FDA.reportPublic FDA data

Right Guard Sport Antiperspirant Unscented

Manufacturer
Thriving Brands LLC
Effective date
2026-01-28
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-06-01 01:35:40

Label at a glance#

ProductRight Guard Sport Antiperspirant Fresh
Active ingredientALUMINUM CHLOROHYDRATE
Label structure20 sections

Label contents#

Full prescribing information#

82699-001

DOSAGE & ADMINISTRATION SECTION

82699-001 Dosage and Administration82699-001 Dosage and Administration

82699-001

WARNINGS SECTION

82699-001 Warnings82699-001 Warnings

82699-001

INACTIVE INGREDIENT SECTION

82699-001 Inactive Ingredient82699-001 Inactive Ingredient

82699-001

INDICATIONS & USAGE SECTION

82699-001 Indications & Usage82699-001 Indications & Usage

82699-002

DOSAGE & ADMINISTRATION SECTION

82699-002 Dosage & Administration82699-002 Dosage & Administration

82699-002

WARNINGS SECTION

82699-002 Warnings82699-002 Warnings

82699-002

INACTIVE INGREDIENT SECTION

82699-002 Inactive Ingredient82699-002 Inactive Ingredient

82699-002

INDICATIONS & USAGE SECTION

82699-002 Indications & Usage82699-002 Indications & Usage

82699-003

DOSAGE & ADMINISTRATION SECTION

82699-003 Dosage & Administration82699-003 Dosage & Administration

82699-003

WARNINGS SECTION

82699-003 Warnings82699-003 Warnings

82699-003

INACTIVE INGREDIENT SECTION

82699-00382699-003

82699-003

INDICATIONS & USAGE SECTION

82699-003 Indications & Usage82699-003 Indications & Usage

82699-001

OTC - ACTIVE INGREDIENT SECTION

82699-001 OTC Active Ingredient82699-001 OTC Active Ingredient

82699-001

OTC - ASK DOCTOR SECTION

82699-001 OTC Ask Doctor82699-001 OTC Ask Doctor

82699-001

OTC - DO NOT USE SECTION

82699-001 Do Not Use82699-001 Do Not Use

82699-001

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

82699-001 OTC-Keep Out of Reach of Children82699-001 OTC-Keep Out of Reach of Children

82699-001

OTC - PURPOSE SECTION

82699-001 OTC Purpose82699-001 OTC Purpose

82699-001

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

82699-001 Package Label Principal Display Panel82699-001 Package Label Principal Display Panel

82699-002

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

82699-002 Package Label Principal Display Panel82699-002 Package Label Principal Display Panel

82699-003

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

82699-003 Package Label Principal Display Panel82699-003 Package Label Principal Display Panel

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
82699-001-01Right Guard Sport Antiperspirant Fresh170 g in 1 CANISTERAEROSOL, SPRAY1704
82699-002-01Right Guard Sport Antiperspirant Powder Dry170 g in 1 CANISTERAEROSOL, SPRAY1704
82699-003-01Right Guard Sport Antiperspirant Unscented170 g in 1 CANISTERAEROSOL, SPRAY1704

Products#

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

DailyMed product names page 1 of 1 · 5 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
82699-00182699-001-01
82699-00282699-002-01
82699-00382699-003-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALUMINUM CHLOROHYDRATEHPN8MZW13MACTIB
CYCLOMETHICONENMQ347994ZIACT
ALUMINUM CHLOROHYDRATEHPN8MZW13MACTIB
CYCLOMETHICONENMQ347994ZIACT
ALUMINUM CHLOROHYDRATEHPN8MZW13MACTIB
CYCLOMETHICONENMQ347994ZIACT

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
Right Guard Sport Antiperspirant FreshRIGHT GUARD SPORT ANTIPERSPIRANT FRESHThriving Brands LLCef5a0215-c94f-60d4-e053-2995a90ace042026-01-28WarningsExact identifier
ndc (package): 82699-003-01
ndc (package): 82699-001-01
ndc (package): 82699-002-01
ndc (product): 82699-001
ndc (product): 82699-002
ndc (product): 82699-003
ndc11 (package): 82699000301
ndc11 (package): 82699000201
ndc11 (package): 82699000101
spl id: 4978ecde-fa38-b3fe-e063-6294a90aeedb
spl set id: ef5a0215-c94f-60d4-e053-2995a90ace04

Reported adverse events (FAERS/openFDA)#

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