AVON ONDUTY 24 HOURS ESSENCE ROLL-ON ANTI-PERSPIRANT DEODORANT- aluminum chlorohydrate stick

AVON OnDuty 24 Hours Essence by

Drug Labeling and Warnings

AVON OnDuty 24 Hours Essence by is a Otc medication manufactured, distributed, or labeled by The Avon Company, Avon Cosmetics Manufacturing, S. de R.L. de C.V.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active ingredient

Aluminum Chlorohydrate 20.0% anhydrous

Purpose

Antiperspirant

Uses

• reduces underarm perspiration

Warnings

For external use only

Do not use on broken skin

Ask a doctor before use if you have kidney disease

Stop use if rash occurs

Keep out of reach of children.
If swallowed, get medical help or contact a Poison Control Center right away.

Directions

• apply to underarms only

Inactive ingredients

WATER, STEARETH-2, PPG-15 STEARYL ETHER, DIISOOCTYL ADIPATE, STEARETH-20, ISOPROPYL PALMITATE, FRAGRANCE

Questions?

Call 1-800-FOR-AVON

To order, contact your Avon Independent Sales Representative or call:
1-800-FOR-AVON www.avon.com

SPL UNCLASSIFIED SECTION

MADE IN MEXICO
DIST. THE AVON COMPANY, NY, NY 10006
©2024 THE AVON COMPANY C2267448

Principal Display Panel

AVON

OnDuty

24
HOURS

ESSENCE

ROLL-ON ANTI-PERSPIRANT DEODORANT

50 ml/1.7 fl.oz. U.S.

INGREDIENTS AND APPEARANCE

AVON ONDUTY 24 HOURS ESSENCE  ROLL-ON ANTI-PERSPIRANT DEODORANT
aluminum chlorohydrate stick

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 10096-1503
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALUMINUM CHLOROHYDRATE (UNII: HPN8MZW13M) (ALUMINUM CHLOROHYDRATE - UNII:HPN8MZW13M)	ALUMINUM CHLOROHYDRATE	200 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
STEARETH-2 (UNII: V56DFE46J5)
WATER (UNII: 059QF0KO0R)
DIISOOCTYL ADIPATE (UNII: 2TLQ9O0CWB)
PPG-15 STEARYL ETHER (UNII: 1II18XLS1L)
STEARETH-20 (UNII: L0Q8IK9E08)
ISOPROPYL PALMITATE (UNII: 8CRQ2TH63M)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 10096-1503-1	50 mL in 1 CONTAINER; Type 0: Not a Combination Product	03/20/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M019	03/20/2024

Labeler - The Avon Company (080143520)

Establishment
Name	Address	ID/FEI	Business Operations
Avon Cosmetics Manufacturing, S. de R.L. de C.V.		815033493	manufacture(10096-1503)