CleanGenic 8 OZ HAND SANITIZER

Manufacturer: CleanGenic, LLC
Effective date: 2023-10-28
Label type: HUMAN OTC DRUG LABEL
Version: 3
Source: full-release
Hydrated at: 2026-05-31 23:58:18

Label at a glance#

ProductCleanGenic 8 OZ HAND SANITIZER

Active ingredientALCOHOL

Label structure7 sections

Indications and uses

For hand sanitizing to decrease bacteria on the skin. Recommended for repeated use.

Dosage and administration

Pump a small amount of foam into palm of hand. Rub thoroughly over all surfaces of both hands. Rub hands briskly together until dry.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethanol 62%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

For hand sanitizing to decrease bacteria on the skin. Recommended for repeated use.

Warnings:

WARNINGS SECTION

Flammable, keep away from fire or flame. For external use only.

When using this product

OTC - WHEN USING SECTION

avoid contact with eyes. In case of eye contact, flush eyes with water.

Stop use and ask a doctor if

OTC - STOP USE SECTION

irritation or redness develops, or if condition persists for more than 72 hours.

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

Pump a small amount of foam into palm of hand. Rub thoroughly over all surfaces of both hands. Rub hands briskly together until dry.

Other Information:

SPL UNCLASSIFIED SECTION

Store below 110° (43°C) May discolor certain fabrics or surfaces.

Inactive Ingredients:

INACTIVE INGREDIENT SECTION

Water, DEA-C8-18 Perfluoroalkylethyl Phosphate, Glycereth-2-Cocoate

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Bottle4

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
616763	ethanol 62 % Topical Foam	PSN	3
616763	ethanol 0.62 ML/ML Topical Foam	SCD	3
616763	ethanol 62 % Topical Foam	SY	3

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
81385-003-08	CleanGenic 8 OZ HAND SANITIZER	24 in 1 BOX	LIQUID	24		3
81385-003-08	CleanGenic 8 OZ HAND SANITIZER	237 mL in 1 BOTTLE	LIQUID	237		3

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
81385-003	CLEANGENIC 8 OZ HAND SANITIZER (ALCOHOL) LIQUID [CLEANGENIC, LLC]	3	Current NDC, Legacy NDC, 2 package rows	20231030_b9828dd7-63a1-0bf4-e053-2a95a90a4569.zip

Products#

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

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

CleanGenic 8 OZ HAND SANITIZER
ALCOHOL
WATER
DIETHANOLAMINE BIS(C8-C18 PERFLUOROALKYLETHYL)PHOSPHATE
GLYCERETH-2 COCOATE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
81385-003	81385-003-08

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
WATER	059QF0KO0R	IACT
DIETHANOLAMINE BIS(C8-C18 PERFLUOROALKYLETHYL)PHOSPHATE	4J55VM509S	IACT
GLYCERETH-2 COCOATE	JWM00VS7HC	IACT
ALCOHOL	3K9958V90M	ACTIB

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
CleanGenic 8 OZ HAND SANITIZER	ALCOHOL	CleanGenic, LLC	b9828dd7-63a1-0bf4-e053-2a95a90a4569	2023-10-28	Warnings	Exact identifier ndc (package): 81385-003-08 ndc (product): 81385-003 ndc11 (package): 81385000308 spl id: 08c00977-1db2-6d24-e063-6294a90a9cfe spl set id: b9828dd7-63a1-0bf4-e053-2a95a90a4569

Reported adverse events (FAERS/openFDA)#

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