EMU Hand Sanitizer Mist Ocean Surf

Manufacturer: EVERYONE MUST USE, LLC
Effective date: 2023-12-22
Label type: HUMAN OTC DRUG LABEL
Version: 3
Source: full-release
Hydrated at: 2026-06-01 00:05:24

Label at a glance#

ProductEMU Hand Sanitizer Mist Ocean Surf

Active ingredientALCOHOL

Label structure9 sections

Indications and uses

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

Dosage and administration

Place enough product on hands to cover all surfaces. Rub hands together until dry. Supervise children under 6 years of age to avoid swallowing.

Storage and handling

Store between 15°-30° C (59°-86°F)

Contacts and useful links#

PhoneLabel contact1-800-250-4643

Label contents#

Full prescribing information#

Purpose

OTC - PURPOSE SECTION

Antiseptic, Hand Sanitizer

Drug Facts

SPL UNCLASSIFIED SECTION

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

*Active Ingredient*	*Purpose*
Alcohol 80% v/v.	Antiseptic

Uses

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. | Contents under pressure.

OTC - DO NOT USE SECTION

Do not use on children less than 2 months of age. Do not use 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.

OTC - STOP USE SECTION

Stop using 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

Place enough product on hands to cover all surfaces. Rub hands together until dry. Supervise children under 6 years of age to avoid swallowing.

Other information

STORAGE AND HANDLING SECTION

Store between 15°-30° C (59°-86°F)

Inactive ingredients

INACTIVE INGREDIENT SECTION

Aloe, Fragrance, Glycerin, Purified Water, Vitamin E

Questions or comments?

OTC - QUESTIONS SECTION

1-800-250-4643

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Net Wt 2.2 FL OZ (62.4g) NDC: 80464-1002-1

Label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
1020364	ethanol 62 % Topical Spray	PSN	3
1020364	ethanol 0.62 ML/ML Topical Spray	SCD	3
1020364	ethanol 62 % Topical Spray	SY	3
1020364	ethyl alcohol 62 % Topical Spray	SY	3

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
80464-1002-1	2024-07-30	C162847	48780-1	0191ceaa-654d-198a-e063-dbdaa90aec3e	EMU Hand Sanitizer Mist Ethyl Alcohol 62% Ocean Surf
80464-1002-1	2023-12-22	C162847	48780-1	0191ceaa-654d-198a-e063-dbdaa90aec3e	EMU Hand Sanitizer Mist Ethyl Alcohol 62% Ocean Surf
80464-1002-1	2023-07-28	C162847	48780-1	0191ceaa-654d-198a-e063-dbdaa90aec3e	EMU Hand Sanitizer Mist Ethyl Alcohol 62% Ocean Surf

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
80464-1002-1	EMU Hand Sanitizer Mist Ocean Surf	62.4 g in 1 BOTTLE, SPRAY	SPRAY	62.4		3

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
80464-1002	EMU HAND SANITIZER MIST OCEAN SURF (ALCOHOL) SPRAY [EVERYONE MUST USE, LLC]	3	Legacy NDC, 1 package rows	20231222_b01b8ce0-4068-2863-e053-2995a90a03e9.zip

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

EMU Hand Sanitizer Mist Ocean Surf
ALCOHOL
GLYCERIN
ALOE
WATER
ALPHA-TOCOPHEROL ACETATE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
80464-1002	80464-1002-1

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
GLYCERIN	PDC6A3C0OX	IACT
ALOE	V5VD430YW9	IACT
WATER	059QF0KO0R	IACT
ALCOHOL	3K9958V90M	ACTIB
ALPHA-TOCOPHEROL ACETATE	9E8X80D2L0	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
0d134903-6e09-f6eb-e063-6394a90a6f5f			b01b8ce0-4068-2863-e053-2995a90a03e9	2023-12-22	Warnings	Exact identifier spl id: 0d134903-6e09-f6eb-e063-6394a90a6f5f spl set id: b01b8ce0-4068-2863-e053-2995a90a03e9

Reported adverse events (FAERS/openFDA)#

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