FDA.reportPublic FDA data

Aluminum Chloride - Clarion Brands, LLC | Inspec Solutions | Inspec Colutions

Manufacturer
Clarion Brands, LLC | Inspec Solutions | Inspec Colutions
Effective date
2026-09-14
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
daily-update
Hydrated at
2026-09-17 01:00:37

Label at a glance#

ProductCertain Dri Clinical Strength Roll On
Active ingredientALUMINUM CHLORIDE
Label structure13 sections

Dosage and administration

apply to underarms only apply at bedtime apply sparingly apply only a few strokes under each arm

Label contents#

Full prescribing information#

Active Ingredient 

OTC - ACTIVE INGREDIENT SECTION

Aluminum chloride 15%

Purpose

OTC - PURPOSE SECTION

Antiperspirant

Use 

INDICATIONS & USAGE SECTION

  • extra effective at reducing underarm perspiration

Warnings

WARNINGS SECTION

For external use only

Do not use

OTC - DO NOT USE SECTION

  • immediately after shaving
  • on broken or irritated skin
  • immediately after bathing

OTC - ASK DOCTOR SECTION

Ask a doctor beforeuse if you have kidney disease

OTC - WHEN USING SECTION

When using this product

  • do not use in or near eyes
  • apply to underarms only

OTC - STOP USE SECTION

Stop use and ask a doctor ifrash or irritation develops

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.

Directions

DOSAGE & ADMINISTRATION SECTION

  • apply to underarms only
  • apply at bedtime
  • apply sparingly
  • apply only a few strokes under each arm

Inactive ingredients

INACTIVE INGREDIENT SECTION

aloe barbadensis leaf juice, artemisia vulgarixs extract, glycerin, hydroxyethylcelluse, laminaria digitata extract, opuntia ficus-indica fruit extract, polyacrylate crosspolymer-6, potassium hydroxide, saccharomyces cerevislae extract, water

OTC - QUESTIONS SECTION

Questions?call 1-844-923-7837

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

Products#

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

DailyMed product names page 1 of 1 · 13 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
69693-72469693-724-03

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 11 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALUMINUM CHLORIDE3CYT62D3GAACTIB
ALOEV5VD430YW9IACT
ARTEMISIA VULGARIS WHOLEJDR81QW9ZQIACT
GLYCERINPDC6A3C0OXIACT
CETYL HYDROXYETHYLCELLULOSE (350000 MW)T7SWE4S2TTIACT
LAMINARIA DIGITATA15E7C67EE8IACT
OPUNTIA FICUS-INDICA FLOWER83YSP51SMAIACT
POLYACRYLATE-1 CROSSPOLYMERR5P9Z5WD6DIACT
POTASSIUM HYDROXIDEWZH3C48M4TIACT
SACCHAROMYCES CEREVISIAE978D8U419HIACT
WATER059QF0KO0RIACT

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
Certain Dri Clinical Strength Roll OnALUMINUM CHLORIDEClarion Brands, LLC076320fa-a765-4c78-a1d4-307b30242f9e2025-12-23WarningsExact identifier
ndc (product): 69693-724

Reported adverse events (FAERS/openFDA)#

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