ANTIPERSPIRANT-DEODORANT ROLL-ON

Manufacturer
CLINIQUE LABORATORIES LLC | Estee Lauder Companies Inc. | Whitman Laboratories Ltd.
Effective date
2023-10-19
Label type
HUMAN OTC DRUG LABEL
Version
10
Source
full-release
Hydrated at
2026-05-31 23:57:03

Label at a glance#

ProductANTIPERSPIRANT-DEODORANT ROLL-ON
Active ingredientALUMINUM CHLOROHYDRATE
Label structure8 sections

Dosage and administration

Apply to underarms only

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Aluminum chlorohydrate 18.20%

Purpose

OTC - PURPOSE SECTION

Antiperspirant

Use

INDICATIONS & USAGE SECTION

Reduces underarm wetness

Warnings

WARNINGS SECTION

For external use only

OTC - DO NOT USE SECTION

Do not use on broken skin

OTC - STOP USE SECTION

Stop use if irritation occurs

OTC - ASK DOCTOR SECTION

Ask a doctor before use if you have kidney disease

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

Inactive ingredients

INACTIVE INGREDIENT SECTION

water\aqua\eau • ceteth-2 • ppg-11 stearyl ether • steareth-20 • myristalkonium chloride • quaternium-14 • sorbic acid • trisodium edta [iln37802]

PRINCIPAL DISPLAY PANEL - 75 ml Bottle Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

C
CLINIQUE

antiperspirant-
deodorant
roll-on

ALUMINUM CHLOROHYDRATE

2.5 FL.OZ.LIQ./75 ml e

PRINCIPAL DISPLAY PANEL - 75 ml Bottle Label
PRINCIPAL DISPLAY PANEL - 75 ml Bottle Label

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
49527-076-012022-08-05C16284748780-1e4f33bdf-ae52-d8a0-e053-dadaa90a6e4eANTIPERSPIRANT-DEODORANT ROLL-ON
49527-076-012022-07-29C16284748780-1e4f33bdf-ae52-d8a0-e053-dadaa90a6e4eANTIPERSPIRANT-DEODORANT ROLL-ON

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
49527-076-01ANTIPERSPIRANT-DEODORANT ROLL-ON75 mL in 1 BOTTLELIQUID7510

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
49527-076ANTIPERSPIRANT-DEODORANT ROLL-ON (ALUMINUM CHLOROHYDRATE) LIQUID [CLINIQUE LABORATORIES LLC]10Current NDC, Legacy NDC, 1 package rows20231020_e496528c-60cf-46ed-9cff-cb4e210a15ab.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
49527-07649527-076-01

Ingredients#

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

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

Source Document#

Source XML · Source PDF

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
ANTIPERSPIRANT-DEODORANT ROLL-ONALUMINUM CHLOROHYDRATECLINIQUE LABORATORIES LLCe496528c-60cf-46ed-9cff-cb4e210a15ab2023-10-19WarningsExact identifier
ndc (package): 49527-076-01
ndc (product): 49527-076
ndc11 (package): 49527007601
spl id: 08167b1b-2efd-1256-e063-6394a90a3eaf
spl set id: e496528c-60cf-46ed-9cff-cb4e210a15ab

Reported adverse events (FAERS/openFDA)#

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