Natural Defense Hand Sanitizer

Manufacturer: Grove Inc.
Effective date: 2020-08-08
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 23:24:16

Label at a glance#

ProductNatural Defense Hand Sanitizer

Active ingredientALCOHOL

Label structure11 sections

Dosage and administration

Our product is made with aloe vera juice, so pour small amount in the palm of your hand & rub in until dry.

Storage and handling

Store between 15-30C (59-86F) Avoid freezing and excessive heat above 40C (104F)

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethanol 66.5% v/v

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

Hand Sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

Warnings

WARNINGS SECTION

For external use only. Flammable. Keep away from heat or flame

Do not use

OTC - DO NOT USE SECTION

in children less than 2 months of age
on open skin wounds

OTC - WHEN USING SECTION

When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.

Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.

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

Our product is made with aloe vera juice, so pour small amount in the palm of your hand & rub in until dry.

Other information

STORAGE AND HANDLING SECTION

Store between 15-30C (59-86F)
Avoid freezing and excessive heat above 40C (104F)

Inactive ingredients

INACTIVE INGREDIENT SECTION

Aloe Vera, Vegetable Glycerin, Vitamin E Oil, Eucalyptus Oil, Lavender Oil, Turmeric Oil, Tea Tree Oil, Jojoba Esters

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
616762	ethanol 66.5 % Topical Gel	PSN	1
616762	ethanol 0.665 ML/ML Topical Gel	SCD	1
616762	ethanol 66.5 % Topical Gel	SY	1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
80004-003-01	2022-01-28	C162847	48780-1	d6a99b39-78fd-a426-e053-dadaa90af4c2	96d3c40a-a8e9-45ad-8102-69c8b54976f0
80004-003-02	2022-01-28	C162847	48780-1	d6a99b39-78fd-a426-e053-dadaa90af4c2	96d3c40a-a8e9-45ad-8102-69c8b54976f0
80004-003-03	2022-01-28	C162847	48780-1	d6a99b39-78fd-a426-e053-dadaa90af4c2	96d3c40a-a8e9-45ad-8102-69c8b54976f0
80004-003-04	2022-01-28	C162847	48780-1	d6a99b39-78fd-a426-e053-dadaa90af4c2	96d3c40a-a8e9-45ad-8102-69c8b54976f0
80004-003-05	2022-01-28	C162847	48780-1	d6a99b39-78fd-a426-e053-dadaa90af4c2	96d3c40a-a8e9-45ad-8102-69c8b54976f0

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
80004-003-01	Natural Defense Hand Sanitizer	59 mL in 1 BOTTLE, PLASTIC	GEL	59	1
80004-003-02	Natural Defense Hand Sanitizer	473 mL in 1 BOTTLE, PLASTIC	GEL	473	1
80004-003-03	Natural Defense Hand Sanitizer	1893 mL in 1 BOTTLE, PLASTIC	GEL	1893	1
80004-003-04	Natural Defense Hand Sanitizer	3785 mL in 1 BOTTLE, PLASTIC	GEL	3785	1
80004-003-05	Natural Defense Hand Sanitizer	1200 mL in 1 BOTTLE, PLASTIC	GEL	1200	1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
80004-003	NATURAL DEFENSE HAND SANITIZER (ALCOHOL) GEL [GROVE INC.]	1	Legacy NDC, 5 package rows	20200811_96d3c40a-a8e9-45ad-8102-69c8b54976f0.zip

Products#

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

DailyMed product names page 1 of 1 · 12 matching rows.

Natural Defense Hand Sanitizer
ALCOHOL
WATER
GLYCERIN
PROPYLENE GLYCOL
ALOE VERA LEAF
CARBOMER HOMOPOLYMER TYPE C (ALLYL PENTAERYTHRITOL CROSSLINKED)
.ALPHA.-TOCOPHEROL ACETATE
EUCALYPTUS OIL
LAVENDER OIL
HYDROLYZED JOJOBA ESTERS (ACID FORM)
TEA TREE OIL

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
80004-003	80004-003-01, 80004-003-02, 80004-003-03, 80004-003-04, 80004-003-05

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 11 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
ALCOHOL	3K9958V90M	ACTIB
WATER	059QF0KO0R	IACT
GLYCERIN	PDC6A3C0OX	IACT
PROPYLENE GLYCOL	6DC9Q167V3	IACT
ALOE VERA LEAF	ZY81Z83H0X	IACT
CARBOMER HOMOPOLYMER TYPE C (ALLYL PENTAERYTHRITOL CROSSLINKED)	4Q93RCW27E	IACT
.ALPHA.-TOCOPHEROL ACETATE	9E8X80D2L0	IACT
EUCALYPTUS OIL	2R04ONI662	IACT
LAVENDER OIL	ZBP1YXW0H8	IACT
HYDROLYZED JOJOBA ESTERS (ACID FORM)	UDR641JW8W	IACT
TEA TREE OIL	VIF565UC2G	IACT

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
0f719a34-d964-4a0e-b5c0-11d3dab8ec1a			96d3c40a-a8e9-45ad-8102-69c8b54976f0	2020-08-08	Warnings	Exact identifier spl id: 0f719a34-d964-4a0e-b5c0-11d3dab8ec1a spl set id: 96d3c40a-a8e9-45ad-8102-69c8b54976f0

Reported adverse events (FAERS/openFDA)#

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