EHS7000

Manufacturer: EPIC Chemistry LLC
Effective date: 2020-09-17
Label type: HUMAN OTC DRUG LABEL
Version: 2
Source: full-release
Hydrated at: 2026-05-31 23:29:39

Label at a glance#

ProductEHS7000

Active ingredientALCOHOL

Label structure10 sections

Indications and uses

Help reduce bacteria on the skin

Dosage and administration

Place a generous amount of product on hands and rub hands together until dry.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 70.05 v/v% Antimicrobial

Uses

OTC - PURPOSE SECTION

Help reduce bacteria on the skin

Warnings

WARNINGS SECTION

For external use only

Flammable. Keep away from heat or flame.

When using this product avoid contact with eyes. If contact occurs, flush thoroughly with water. Avoid contact with broken skin. Do not ingest or inhale.

Stop use and ask doctor if skin irritation or redness occurs.

Keep out of reach of children. If swallowed, seek medical attention or contact Poison Control Center immediately.

Directions

INSTRUCTIONS FOR USE SECTION

Place a generous amount of product on hands and rub hands together until dry.

Other information

OTHER SAFETY INFORMATION

Do not store above 100° F. May cause fabric discoloration.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water (Agua), Sorbitol, Methycellulose, Polyquaternium-10, Fragrance, Glycerin

Dosage

DOSAGE & ADMINISTRATION SECTION

Use a liberal amount in palm of hand.

Notice

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

Indications & Usage

INDICATIONS & USAGE SECTION

For use when soap and water are not available, or in addition to.

Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
77022-1113-8	2022-01-28	C162847	48780-1	d6a99b39-4732-a426-e053-dadaa90af4c2	8 OZ

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
77022-1113-8	EHS7000	1 in 1 BOTTLE	GEL	1		2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
77022-1113	EHS7000 GEL [EPIC CHEMISTRY LLC]	2	Legacy NDC, 1 package rows	20200918_aee8d065-2701-55df-e053-2a95a90a3dda.zip

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

EHS7000
ALCOHOL
WATER
METHYLCELLULOSE, UNSPECIFIED
POLYQUATERNIUM-10 (30000 MPA.S AT 2%)
SORBITOL
GLYCERIN

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
77022-1113	77022-1113-8

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
ALCOHOL	3K9958V90M	ACTIB
WATER	059QF0KO0R	IACT
METHYLCELLULOSE, UNSPECIFIED	Z944H5SN0H	IACT
POLYQUATERNIUM-10 (30000 MPA.S AT 2%)	C7RDC8Y4JS	IACT
SORBITOL	506T60A25R	IACT
GLYCERIN	PDC6A3C0OX	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
af83c285-fb8b-b98e-e053-2a95a90a0476			aee8d065-2701-55df-e053-2a95a90a3dda	2020-09-17	Warnings	Exact identifier spl id: af83c285-fb8b-b98e-e053-2a95a90a0476 spl set id: aee8d065-2701-55df-e053-2a95a90a3dda

Reported adverse events (FAERS/openFDA)#

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