FDA.reportPublic FDA data

On Duty Unscented

Manufacturer
New Avon LLC
Effective date
2019-01-01
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-05-31 22:58:59

Label at a glance#

ProductOn Duty Unscented Roll-On Anti-Perspirant Deodorant
Active ingredientALUMINUM CHLOROHYDRATE
Label structure7 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredient

Aluminum Chlorohydrate 20.7%, anhydrous........

OTC - PURPOSE SECTION

Purpose

........Antiperspirant

INDICATIONS & USAGE SECTION

Uses

  • reduces underarm perspiration
  • lasts 24 hours

WARNINGS SECTION

Warnings

For external use only

OTC - WHEN USING SECTION

When using this product

  • do not apply to broken skin
  • stop use if rash or irritation develops
OTC - ASK DOCTOR SECTION

Ask a doctor before use

  • if you have kidney disease
Keep out of reach of childrenIf swallowed, get medical help or contact a Poison Control Center right away.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

DOSAGE & ADMINISTRATION SECTION

Directions

  • apply to underarms only

INACTIVE INGREDIENT SECTION

Inactive ingredients

Water/Eau, PPG-15 Stearyl Ether, Steareth-2, Diisopropyl Adipate, Steareth-20.

OTC - QUESTIONS SECTION

Questions?

Call 1-800-FOR-AVON or 1-800-265-AVON in Canada

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image of labelimage of labelimage of DFBimage of DFBimage of DFBimage of DFBimage of DFBimage of DFB

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
10096-5219-12021-01-29C16284748780-1ba0f9c33-43fb-a910-e053-dadaa90a0b85On Duty Anti-Perspirant Roll-On Deodorant (Unscented)
10096-5219-22021-01-29C16284748780-1ba0f9c33-43fb-a910-e053-dadaa90a0b85On Duty Anti-Perspirant Roll-On Deodorant (Unscented)

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
10096-5219-1On Duty UnscentedRoll-On Anti-Perspirant Deodorant50 mL in 1 BOTTLE, DISPENSINGGEL504
10096-5219-2On Duty UnscentedRoll-On Anti-Perspirant Deodorant75 mL in 1 BOTTLE, DISPENSINGGEL754

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
10096-5219ON DUTY UNSCENTED ROLL-ON ANTI-PERSPIRANT DEODORANT (ALUMINUM CHLOROHYDRATE) GEL [NEW AVON LLC]4Legacy NDC, 2 package rows20190328_0cee1616-bdc4-41b7-b230-26d9dbfec3ee.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
ALUMINUM CHLOROHYDRATEACTIVE INGREDIENTHPN8MZW13M1
ALUMINUM CHLOROHYDRATEACTIVE MOIETYHPN8MZW13M1

Products#

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

DailyMed product names page 1 of 1 · 3 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
10096-521910096-5219-1, 10096-5219-2

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALUMINUM CHLOROHYDRATEHPN8MZW13MACTIB
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
85171b5e-a3aa-1613-e053-2991aa0ab02f0cee1616-bdc4-41b7-b230-26d9dbfec3ee2019-01-01WarningsExact identifier
spl id: 85171b5e-a3aa-1613-e053-2991aa0ab02f
spl set id: 0cee1616-bdc4-41b7-b230-26d9dbfec3ee

Reported adverse events (FAERS/openFDA)#

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