Naturals

Manufacturer: Avon Products, Inc.
Effective date: 2010-06-11
Label type: HUMAN OTC DRUG LABEL
Version: 2
Source: full-release
Hydrated at: 2026-05-31 22:25:12

Label at a glance#

ProductNaturals Vanilla Anti-Perspirant Deodorant

Active ingredientAluminum Chlorohydrate

Label structure7 sections

Contacts and useful links#

PhoneLabel contact1-800-FOR-AVON

PhoneLabel contact1-800-265-AVON

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active/
Medicinal ingredient Purpose
Aluminum Chlorohydrate
14.5%, anhydrous...................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

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.

DOSAGE & ADMINISTRATION SECTION

Directions
• apply to underarms only

INACTIVE INGREDIENT SECTION

Inactive/Non-medicinal ingredients:

     WATER/EAU
     STEARETH-2
     PPG-15 STEARYL ETHER
     GLYCINE SOJA (SOYBEAN) SEED EXTRACT
     VANILLA PLANIFOLIA FRUIT EXTRACT
     HYDROLYZED MILK PROTEIN
     DICAPRYL ADIPATE
     STEARETH-20
     ISOPROPYL PALMITATE
     PARFUM/FRAGRANCE

OTC - QUESTIONS SECTION

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

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image of PDPimage of back label

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
10096-0217-1	2019-10-21	C162847	48780-1	956f9ecf-cf72-621f-e053-dbdaa90a74ad	Drug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
10096-0217-1	NaturalsVanilla Anti-Perspirant Deodorant	50 mL in 1 BOTTLE, DISPENSING	GEL	50		2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
10096-0217	NATURALS VANILLA ANTI-PERSPIRANT DEODORANT (ALUMINUM CHLOROHYDRATE) GEL [AVON PRODUCTS, INC.]	2	Legacy NDC, 1 package rows	20100714_a83012c8-2451-4b66-b2f7-2aec92879aca.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	SPL version
Aluminum Chlorohydrate	ACTIVE INGREDIENT	HPN8MZW13M	2
ALUMINUM CATION	ACTIVE MOIETY	3XHB1D032B	2
ISOPROPYL PALMITATE	INACTIVE INGREDIENT	8CRQ2TH63M	2
STEARETH-2	INACTIVE INGREDIENT	V56DFE46J5	2
STEARETH-20	INACTIVE INGREDIENT	L0Q8IK9E08	2
WATER	INACTIVE INGREDIENT	059QF0KO0R	2

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

Naturals Vanilla Anti-Perspirant Deodorant
Aluminum Chlorohydrate
ALUMINUM CATION
WATER
STEARETH-2
STEARETH-20
ISOPROPYL PALMITATE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
10096-0217	10096-0217-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
Aluminum Chlorohydrate	HPN8MZW13M	ACTIB
WATER	059QF0KO0R	IACT
STEARETH-2	V56DFE46J5	IACT
STEARETH-20	L0Q8IK9E08	IACT
ISOPROPYL PALMITATE	8CRQ2TH63M	IACT

Source Document#

Source XML

Inactive ingredient matches#

Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.

Inactive ingredient links page 1 of 1 · 13 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredient	IID ingredient	UNII	Dosage form / route	Potency	Maximum daily exposure	Match
ISOPROPYL PALMITATE	ISOPROPYL PALMITATE	8CRQ2TH63M	FILM, EXTENDED RELEASE / TRANSDERMAL	187.5 mg		Exact identifier — unii candidate 8 equally ranked IID candidates
ISOPROPYL PALMITATE	ISOPROPYL PALMITATE	8CRQ2TH63M	CREAM / TOPICAL		112 mg	Exact identifier — unii candidate 8 equally ranked IID candidates
ISOPROPYL PALMITATE	ISOPROPYL PALMITATE	8CRQ2TH63M	GEL / TOPICAL	NA		Exact identifier — unii candidate 8 equally ranked IID candidates
ISOPROPYL PALMITATE	ISOPROPYL PALMITATE	8CRQ2TH63M	FILM / TRANSDERMAL		2 mg	Exact identifier — unii candidate 8 equally ranked IID candidates
STEARETH-2	STEARETH-2	V56DFE46J5	LOTION / TOPICAL	0.4 %w/w		Exact identifier — unii candidate 4 equally ranked IID candidates
ISOPROPYL PALMITATE	ISOPROPYL PALMITATE	8CRQ2TH63M	AEROSOL / TOPICAL		397 mg	Exact identifier — unii candidate 8 equally ranked IID candidates
STEARETH-20	STEARETH-20	L0Q8IK9E08	CREAM / TOPICAL	4.15 %w/w		Exact identifier — unii candidate
ISOPROPYL PALMITATE	ISOPROPYL PALMITATE	8CRQ2TH63M	OINTMENT / TOPICAL	NA		Exact identifier — unii candidate 8 equally ranked IID candidates
STEARETH-2	STEARETH-2	V56DFE46J5	OINTMENT / TOPICAL		714 mg	Exact identifier — unii candidate 4 equally ranked IID candidates
STEARETH-2	STEARETH-2	V56DFE46J5	AEROSOL, FOAM / TOPICAL	1.09 %w/w		Exact identifier — unii candidate 4 equally ranked IID candidates
ISOPROPYL PALMITATE	ISOPROPYL PALMITATE	8CRQ2TH63M	LOTION / TOPICAL	5 %w/w		Exact identifier — unii candidate 8 equally ranked IID candidates
STEARETH-2	STEARETH-2	V56DFE46J5	CREAM / TOPICAL		643 mg	Exact identifier — unii candidate 4 equally ranked IID candidates
ISOPROPYL PALMITATE	ISOPROPYL PALMITATE	8CRQ2TH63M	AEROSOL, SPRAY / TOPICAL		397 mg	Exact identifier — unii candidate 8 equally ranked IID candidates

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
2d7176bc-35f2-4365-9bad-1378673c387f			a83012c8-2451-4b66-b2f7-2aec92879aca	2010-06-11	Warnings	Exact identifier spl id: 2d7176bc-35f2-4365-9bad-1378673c387f spl set id: a83012c8-2451-4b66-b2f7-2aec92879aca

Reported adverse events (FAERS/openFDA)#

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