EQUINOX

Manufacturer: ATA FOOD LTD LIABILITY CO
Effective date: 2020-06-29
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 23:19:37

Label at a glance#

ProductEQUINOX

Active ingredientALCOHOL

Label structure9 sections

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 o C (59-86 o F). Avoid freezing and excessive heat above 40 o C (104 o F).

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Alcohol 70% 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

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

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

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^oC (59-86^oF).
Avoid freezing and excessive heat above 40^oC (104^oF).

Inactive ingredients

INACTIVE INGREDIENT SECTION

Deionized water, glycerin, hydrogen peroxide.

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
581662	ethanol 70 % Topical Gel	PSN	1
581662	ethanol 0.7 ML/ML Topical Gel	SCD	1
581662	ethanol 70 % Topical Gel	SY	1
581662	ethyl alcohol 70 % Topical Gel	SY	1

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
79229-001-01	2022-01-28	C162847	48780-1	d6a99b39-5b47-a426-e053-dadaa90af4c2	8b459120-648c-4525-ba71-c204076ad619
79229-001-02	2022-01-28	C162847	48780-1	d6a99b39-5b47-a426-e053-dadaa90af4c2	8b459120-648c-4525-ba71-c204076ad619
79229-001-03	2022-01-28	C162847	48780-1	d6a99b39-5b47-a426-e053-dadaa90af4c2	8b459120-648c-4525-ba71-c204076ad619
79229-001-04	2022-01-28	C162847	48780-1	d6a99b39-5b47-a426-e053-dadaa90af4c2	8b459120-648c-4525-ba71-c204076ad619
79229-001-05	2022-01-28	C162847	48780-1	d6a99b39-5b47-a426-e053-dadaa90af4c2	8b459120-648c-4525-ba71-c204076ad619
79229-001-06	2022-01-28	C162847	48780-1	d6a99b39-5b47-a426-e053-dadaa90af4c2	8b459120-648c-4525-ba71-c204076ad619
79229-001-07	2022-01-28	C162847	48780-1	d6a99b39-5b47-a426-e053-dadaa90af4c2	8b459120-648c-4525-ba71-c204076ad619
79229-001-08	2022-01-28	C162847	48780-1	d6a99b39-5b47-a426-e053-dadaa90af4c2	8b459120-648c-4525-ba71-c204076ad619

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
79229-001-01	EQUINOX	100 mL in 1 DRUM	LIQUID	100	1
79229-001-02	EQUINOX	200 mL in 1 DRUM	LIQUID	200	1
79229-001-03	EQUINOX	500 mL in 1 BOTTLE, PLASTIC	LIQUID	500	1
79229-001-04	EQUINOX	1000 mL in 1 DRUM	LIQUID	1000	1
79229-001-05	EQUINOX	5000 mL in 1 DRUM	LIQUID	5000	1
79229-001-06	EQUINOX	10000 mL in 1 DRUM	LIQUID	10000	1
79229-001-07	EQUINOX	20000 mL in 1 DRUM	LIQUID	20000	1
79229-001-08	EQUINOX	30000 mL in 1 DRUM	LIQUID	30000	1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
79229-001	EQUINOX (ALCOHOL) LIQUID [ATA FOOD LTD LIABILITY CO]	1	Legacy NDC, 8 package rows	20200701_8b459120-648c-4525-ba71-c204076ad619.zip

Products#

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

DailyMed product names page 1 of 1 · 5 matching rows.

EQUINOX
Alcohol
GLYCERIN
WATER
HYDROGEN PEROXIDE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
79229-001	79229-001-01, 79229-001-02, 79229-001-03, 79229-001-04, 79229-001-05, 79229-001-06, 79229-001-07, 79229-001-08

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
ALCOHOL	3K9958V90M	ACTIB
GLYCERIN	PDC6A3C0OX	IACT
WATER	059QF0KO0R	IACT
HYDROGEN PEROXIDE	BBX060AN9V	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
0378c237-8ead-49c0-9e9f-c88b2f69ac6f			8b459120-648c-4525-ba71-c204076ad619	2020-06-29	Warnings	Exact identifier spl id: 0378c237-8ead-49c0-9e9f-c88b2f69ac6f spl set id: 8b459120-648c-4525-ba71-c204076ad619

Reported adverse events (FAERS/openFDA)#

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