SONO

Manufacturer: Advanced Ultrasound Solutions Inc.
Effective date: 2020-09-09
Label type: HUMAN OTC DRUG LABEL
Version: 2
Source: full-release
Hydrated at: 2026-05-31 23:32:15

Label at a glance#

ProductSONO

Active ingredientALCOHOL

Label structure8 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 when using this product to avoid swallowing.

Storage and handling

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

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 70%v/v

Purpose

OTC - PURPOSE SECTION

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

Do not use

OTC - DO NOT USE SECTION

on children less than 2 months of age
on open skin wound

When using this product

OTC - WHEN USING SECTION

keep out of reach of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.

Stop use and ask a doctor

OTC - STOP USE SECTION

if irritation or rash occurs. These may be signs of a serious condition.

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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 when using this product to avoid swallowing.

Other information

STORAGE AND HANDLING SECTION

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

Inactive ingredients

INACTIVE INGREDIENT SECTION

acrylates/C10 30 alkyl acrylate crosspolymer, fragrance (parfum), glycerin, aminomethyl propanol, carbomer, hydrogen peroxide, water (aqua).

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC: 77677-002-02, 77677-002-08, 77677-002-16, 77677-002-01

SONO^® HEALTHCARE

MADE IN USA

70% ALCOHOL

HAND SANITIZER

KILLS 99.99% OF MOST COMMON GERMS

SULFATE FREE - PARABEN FREE

e 60 ml | 2 fl oz

e 236 ml | 8 fl oz

e 472 ml | 16 fl oz

e 3785 ml | 1 gallon

Label

Label 1

Label 2

Label 3

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
582753	ethanol 70 % Topical Solution	PSN	2
582753	ethanol 0.7 ML/ML Topical Solution	SCD	2
582753	ethanol 70 % Topical Solution	SY	2
582753	ethyl alcohol 70 % Topical Solution	SY	2

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
5eb9f24b-9328-475e-af0a-18021935eb6a	Product name	1	20180220

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
77677-002-01	2022-01-28	C162847	48780-1	d6a99b39-4781-a426-e053-dadaa90af4c2	Drug Facts
77677-002-02	2022-01-28	C162847	48780-1	d6a99b39-4781-a426-e053-dadaa90af4c2	Drug Facts
77677-002-08	2022-01-28	C162847	48780-1	d6a99b39-4781-a426-e053-dadaa90af4c2	Drug Facts
77677-002-16	2022-01-28	C162847	48780-1	d6a99b39-4781-a426-e053-dadaa90af4c2	Drug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
77677-002-01	SONO	3785 mL in 1 PACKAGE	SOLUTION	3785	2
77677-002-02	SONO	60 mL in 1 BOTTLE	SOLUTION	60	2
77677-002-08	SONO	236 mL in 1 BOTTLE	SOLUTION	236	2
77677-002-16	SONO	473 mL in 1 BOTTLE	SOLUTION	473	2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
77677-002	SONO (ETHYL ALCOHOL) SOLUTION [ADVANCED ULTRASOUND SOLUTIONS INC.]	2	Legacy NDC, 4 package rows	20201023_266eb595-1062-49d2-ab2d-0ad1ed68c7aa.zip

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

SONO
Ethyl Alcohol
ALCOHOL
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED)
GLYCERIN
AMINOMETHYLPROPANOL
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE
HYDROGEN PEROXIDE
WATER

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
77677-002	77677-002-02, 77677-002-08, 77677-002-16, 77677-002-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
ALCOHOL	3K9958V90M	ACTIB
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED)	59TL3WG5CO	IACT
GLYCERIN	PDC6A3C0OX	IACT
AMINOMETHYLPROPANOL	LU49E6626Q	IACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE	0A5MM307FC	IACT
HYDROGEN PEROXIDE	BBX060AN9V	IACT
WATER	059QF0KO0R	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
8b67ac1f-a4b2-4cfc-b2b4-e9b9b5eb5621			266eb595-1062-49d2-ab2d-0ad1ed68c7aa	2020-09-09	Warnings	Exact identifier spl id: 8b67ac1f-a4b2-4cfc-b2b4-e9b9b5eb5621 spl set id: 266eb595-1062-49d2-ab2d-0ad1ed68c7aa

Reported adverse events (FAERS/openFDA)#

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