ELLE ANTIBACTERIAL HAND WIPES

Manufacturer: Alta Sales Inc
Effective date: 2020-08-27
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 23:26:17

Label at a glance#

ProductELLE ANTIBACTERIAL HAND WIPES

Active ingredientBENZALKONIUM CHLORIDE

Label structure8 sections

Dosage and administration

Thoroughly wipe hands and face as desired. Allow to dry without wiping. Discard wipe in trash receptacle after use. Do not flush.

Contacts and useful links#

Websitewww.ellepersonalcare.us

www.ellepersonalcare.us

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.13%

Purpose

OTC - PURPOSE SECTION

Antibacterial

INDICATIONS & USAGE SECTION

Use • Decreases bacteria on skin

Warnings

WARNINGS SECTION

For external use only

Keep out of eyes. In case of eye contact, rinse with water.

If irritation develops, discontinue use.

Consult a doctor if irritation persists more than 72 hours.

If swallowed, seek medical attention or contact a Poison Control Center.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of the children, except with adult supervision.

Directions for use

DOSAGE & ADMINISTRATION SECTION

Thoroughly wipe hands and face as desired.

Allow to dry without wiping.

Discard wipe in trash receptacle after use. Do not flush.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Aqua, Phenoxyethanol, Perfume, Propylene Glycol, Cocamidopropyl Betaine, PEG-7 Glyceryl Cocoate, Benzoic acid, Tetrasodium Edta, Dehydroacetic acid, Glycerin, Polysorbate 20, Citric acid

SPL UNCLASSIFIED SECTION

KILLS 99.99% OF GERMS

HYPOALLERGENIC • PARABEN FREE

DERMATOLOGICALLY TESTED

ELLE_™

is used by Alta Sales Inc under license

from HACHETTE FILIPACCHI PRESSE

SA, Paris, France.

Made in Turkey

www.ellepersonalcare.us

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PackagingPackaging

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
1038558	benzalkonium chloride 0.13 % Medicated Pad	PSN	1
1038558	benzalkonium chloride 1.3 MG/ML Medicated Pad	SCD	1
1038558	benzalkonium chloride 0.13 % Topical Cloth	SY	1
1038558	benzalkonium chloride 0.13 % Topical Swab	SY	1
1038558	benzalkonium chloride 0.13 GM per 100 GM Topical Pad	SY	1
1038558	benzalkonium chloride 0.13 GM per 100 GM Topical Swab	SY	1
1038558	benzalkonium chloride 1 ML per 750 ML Topical Swab	SY	1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
79165-111-20	2022-01-28	C162847	48780-1	d6a99b39-609d-a426-e053-dadaa90af4c2	ELLE ANTIBACTERIAL HAND WIPES
79165-111-80	2022-01-28	C162847	48780-1	d6a99b39-609d-a426-e053-dadaa90af4c2	ELLE ANTIBACTERIAL HAND WIPES
79165-111-90	2022-01-28	C162847	48780-1	d6a99b39-609d-a426-e053-dadaa90af4c2	ELLE ANTIBACTERIAL HAND WIPES

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
79165-111-20	ELLE ANTIBACTERIAL HAND WIPES	3.6 g in 1 PACKAGE	CLOTH	3.6	1
79165-111-20	ELLE ANTIBACTERIAL HAND WIPES	20 in 1 PACKET	CLOTH	20	1
79165-111-80	ELLE ANTIBACTERIAL HAND WIPES	80 in 1 PACKET	CLOTH	80	1
79165-111-80	ELLE ANTIBACTERIAL HAND WIPES	3.6 g in 1 PACKAGE	CLOTH	3.6	1
79165-111-90	ELLE ANTIBACTERIAL HAND WIPES	3.6 g in 1 PACKAGE	CLOTH	3.6	1
79165-111-90	ELLE ANTIBACTERIAL HAND WIPES	90 in 1 PACKET	CLOTH	90	1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
79165-111	ELLE ANTIBACTERIAL HAND WIPES (BENZALKONIUM CHLORIDE) CLOTH [ALTA SALES INC]	1	Legacy NDC, 6 package rows	20200829_fc09f27d-7549-4111-ae2d-0657b229653a.zip

Products#

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

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

ELLE ANTIBACTERIAL HAND WIPES
BENZALKONIUM CHLORIDE
BENZALKONIUM
WATER
PHENOXYETHANOL
PROPYLENE GLYCOL
COCAMIDOPROPYL BETAINE
PEG-7 GLYCERYL COCOATE
BENZOIC ACID
EDETATE SODIUM
DEHYDROACETIC ACID
GLYCERIN
POLYSORBATE 20
CITRIC ACID MONOHYDRATE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
79165-111	79165-111-20, 79165-111-80, 79165-111-90

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 12 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
BENZALKONIUM CHLORIDE	F5UM2KM3W7	ACTIB
WATER	059QF0KO0R	IACT
PHENOXYETHANOL	HIE492ZZ3T	IACT
PROPYLENE GLYCOL	6DC9Q167V3	IACT
COCAMIDOPROPYL BETAINE	5OCF3O11KX	IACT
PEG-7 GLYCERYL COCOATE	VNX7251543	IACT
BENZOIC ACID	8SKN0B0MIM	IACT
EDETATE SODIUM	MP1J8420LU	IACT
DEHYDROACETIC ACID	2KAG279R6R	IACT
GLYCERIN	PDC6A3C0OX	IACT
POLYSORBATE 20	7T1F30V5YH	IACT
CITRIC ACID MONOHYDRATE	2968PHW8QP	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
dcfa103e-80cd-4539-9650-002f3e858c52			fc09f27d-7549-4111-ae2d-0657b229653a	2020-08-27	Warnings	Exact identifier spl id: dcfa103e-80cd-4539-9650-002f3e858c52 spl set id: fc09f27d-7549-4111-ae2d-0657b229653a

Reported adverse events (FAERS/openFDA)#

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