Hand Essentials Antibacterial

Manufacturer: Hu-Friedy Mfg. Co. LLC | Vintage Chemical Inc
Effective date: 2020-06-04
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 23:16:33

Label at a glance#

ProductHand Essentials Antibacterial

Active ingredientCHLOROXYLENOL

Label structure7 sections

Dosage and administration

Ready to use. Do not dilute. Wet hands and forearms. Apply 5 ml (tsp) or palmful to hands and forearms. Scrub thoroughly for 1 minute and rinse.

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

PCMX (para-chloro-meta-xylenol) 0.6%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

for handwashing to decrease bacteria on skin

Warnings

WARNINGS SECTION

For external use only.

OTC - WHEN USING SECTION

When using this product:

Do not get in eyes.
If contact occurs, rinse eyes thoroughly with water.

OTC - STOP USE SECTION

Stop use and ask a doctor if

irritation and redness develop.

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

Ready to use.
Do not dilute.
Wet hands and forearms.
Apply 5 ml (tsp) or palmful to hands and forearms.
Scrub thoroughly for 1 minute and rinse.

Inert ingredients

INACTIVE INGREDIENT SECTION

Water, Sodium Lauryl Sulfate, Sodium Laureth Sulfate, Cocamidopropylbetaine, Tetrasodium EDTA, Propylene Glycol, Fragrance, Sodium Chloride, Boric Acid, Glycol Stearate, PEG-75 Lanolin, DMDM Hydantoin, Aloe Vera.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Hu-Friedy

HAND ESSENTIALS

ANTIBACTERIAL SOAP

Effective against a broad

spectrum of activity

against gram negative and

gram positive bacteria.

Contains emollients to

help moisten skin and

maintain its natural oils.

473 ml/16.0 FL. OZ.

NDC: 65626-018-16

Manufactured for:

Hu-Friedy Nfg. Co., LLC

3232 N. Rockwell St. Chicago, IL 60618

1-800-Hu-Friedy Hu-Friedy.com

MADE IN USA

Hu-Friedy

container labela

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
413262	chloroxylenol 0.6 % Medicated Liquid Soap	PSN	1
413262	chloroxylenol 6 MG/ML Medicated Liquid Soap	SCD	1
413262	chloroxylenol 0.6 % Medicated Liquid Soap	SY	1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
65626-018-16	2022-01-28	C162847	48780-1	d6a99b39-c1a7-a426-e053-dadaa90af4c2	a746f7a6-72e5-469a-e053-2995a90a90a3

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
65626-018-16	Hand Essentials Antibacterial	473 mL in 1 BOTTLE, PUMP	SOAP	473		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
65626-018	HAND ESSENTIALS ANTIBACTERIAL (CHLOROXYLENOL) SOAP [HU-FRIEDY MFG. CO. LLC]	1	Legacy NDC, 1 package rows	20200609_a746f7a6-72e5-469a-e053-2995a90a90a3.zip

Products#

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

DailyMed product names page 1 of 1 · 14 matching rows.

Hand Essentials Antibacterial
CHLOROXYLENOL
WATER
SODIUM LAURETH SULFATE
COCAMIDOPROPYL BETAINE
EDETATE SODIUM
PROPYLENE GLYCOL
SODIUM CHLORIDE
BORIC ACID
PEG-75 LANOLIN
DMDM HYDANTOIN
SODIUM LAURYL SULFATE
GLYCOL STEARATE
ALOE VERA LEAF

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
65626-018	65626-018-16

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 13 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
CHLOROXYLENOL	0F32U78V2Q	ACTIB
WATER	059QF0KO0R	IACT
SODIUM LAURETH SULFATE	BPV390UAP0	IACT
COCAMIDOPROPYL BETAINE	5OCF3O11KX	IACT
EDETATE SODIUM	MP1J8420LU	IACT
PROPYLENE GLYCOL	6DC9Q167V3	IACT
SODIUM CHLORIDE	451W47IQ8X	IACT
BORIC ACID	R57ZHV85D4	IACT
PEG-75 LANOLIN	09179OX7TB	IACT
DMDM HYDANTOIN	BYR0546TOW	IACT
SODIUM LAURYL SULFATE	368GB5141J	IACT
GLYCOL STEARATE	0324G66D0E	IACT
ALOE VERA LEAF	ZY81Z83H0X	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
a746f7a6-72e6-469a-e053-2995a90a90a3			a746f7a6-72e5-469a-e053-2995a90a90a3	2020-06-04	Warnings	Exact identifier spl id: a746f7a6-72e6-469a-e053-2995a90a90a3 spl set id: a746f7a6-72e5-469a-e053-2995a90a90a3

Reported adverse events (FAERS/openFDA)#

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