Naturals

Manufacturer: New Avon LLC | Avon Products, Inc.
Effective date: 2016-02-16
Label type: HUMAN OTC DRUG LABEL
Version: 3
Source: full-release
Hydrated at: 2026-05-31 22:45:18

Label at a glance#

ProductNaturals Vanilla Antibacterial Hand

Active ingredientALCOHOL

Label structure7 sections

Contacts and useful links#

PhoneLabel contact1-800-FOR-AVON

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient

Ethyl Alcohol 64.76%.......................

OTC - PURPOSE SECTION

Purpose

...............Antiseptic

INDICATIONS & USAGE SECTION

Uses

For handwashing to decrease bacteria on the skin

WARNINGS SECTION

Warnings
For external use only

OTC - WHEN USING SECTION

When using this product

Avoid contact with eyes. If contact occurs, rinse thoroughly with water.

OTC - ASK DOCTOR SECTION

Stop use and ask a health care practitioner if

irritation and redness develop

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 immediately.

GENERAL PRECAUTIONS SECTION

FLAMMABLE. Keep away from open flame and sources of heat.

DOSAGE & ADMINISTRATION SECTION

Directions

Wet hands thoroughly with product and allow to dry without wiping.

INACTIVE INGREDIENT SECTION

Inactive ingredients

     WATER/EAU
     GLYCERIN
     VANILLA PLANIFOLIA FRUIT EXTRACT
     GLYCINE SOJA (SOYBEAN) SEED EXTRACT
     PARFUM/FRAGRANCE
     HYDROXYPROPYLCELLULOSE
     CARBOMER
     TRIETHANOLAMINE

OTC - QUESTIONS SECTION

Questions? Call 1-800-FOR-AVON

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image of PDPimage of labelimage of label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
902574	ethanol 65 % Topical Gel	PSN	3
902574	ethanol 0.65 ML/ML Topical Gel	SCD	3
902574	ethyl alcohol 65 % Topical Gel	SY	3

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
10096-0251-1	2020-01-31	C162847	48780-1	9d75b9d0-e236-f424-e053-dadaa90a57ce	a993a6e7-4728-4b0c-98ca-805ff65cdcbd
10096-0251-2	2020-01-31	C162847	48780-1	9d75b9d0-e236-f424-e053-dadaa90a57ce	a993a6e7-4728-4b0c-98ca-805ff65cdcbd

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
10096-0251-1	NaturalsVanilla Antibacterial Hand	30 mL in 1 BOTTLE	GEL	30		3
10096-0251-2	NaturalsVanilla Antibacterial Hand	75 mL in 1 TUBE	GEL	75		3

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
10096-0251	NATURALS VANILLA ANTIBACTERIAL HAND (ALCOHOL) GEL [NEW AVON LLC]	3	Legacy NDC, 2 package rows	20160303_a993a6e7-4728-4b0c-98ca-805ff65cdcbd.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	SPL version	Uploaded
ALCOHOL	ACTIVE INGREDIENT	3K9958V90M	2
ALCOHOL	ACTIVE MOIETY	3K9958V90M	2

Products#

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

DailyMed product names page 1 of 1 · 2 matching rows.

Naturals Vanilla Antibacterial Hand
Alcohol

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
10096-0251	10096-0251-1, 10096-0251-2

Ingredients#

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

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

Name, UNII, Kind table
Name	UNII	Kind
ALCOHOL	3K9958V90M	ACTIB

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
2fe00e0d-e134-4a3d-adce-c8627c1f22cd			a993a6e7-4728-4b0c-98ca-805ff65cdcbd	2016-02-16	Warnings	Exact identifier spl id: 2fe00e0d-e134-4a3d-adce-c8627c1f22cd spl set id: a993a6e7-4728-4b0c-98ca-805ff65cdcbd

Reported adverse events (FAERS/openFDA)#

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