Walgreens

Manufacturer: WALGREEN COMPANY | APOLLO HEALTH AND BEAUTY CARE INC.
Effective date: 2022-09-12
Label type: HUMAN OTC DRUG LABEL
Version: 3
Source: full-release
Hydrated at: 2026-05-31 23:50:38

Label at a glance#

ProductWalgreens ANTIBACTERIAL HAND REFILL

Active ingredientBENZALKONIUM CHLORIDE

Label structure8 sections

Indications and uses

Helps eliminate bacteria on hands

Dosage and administration

use to refill a hand soap pump bottle from pump bottle, apply onto wet hands lather and rinse thoroughly

Storage and handling

store at room temperature

Contacts and useful links#

PhoneLabel contact1-800-925-4733

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.13%

Purpose

OTC - PURPOSE SECTION

Antibacterial

Uses

INDICATIONS & USAGE SECTION

Helps eliminate bacteria on hands

Warnings

WARNINGS SECTION

For external use only.

When using this product

OTC - WHEN USING SECTION

avoid contact with eyes. In case of contact, rinse thoroughly with water.

Stop use and ask doctor if

OTC - STOP USE SECTION

irritation or redness develops and lasts.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

In case of accidental ingestion, get medical help or contact a Poison Control Center immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

use to refill a hand soap pump bottle
from pump bottle, apply onto wet hands
lather and rinse thoroughly

Other informaton

STORAGE AND HANDLING SECTION

store at room temperature

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water (Aqua), Lauramidopropylamine Oxide, Glycerin, Cetrimonium Chloride, Sodium Chloride, Cocamide MEA, PEG-120 Methyl Glucose Dioleate, Fragrance (Parfum), Citric Acid, Tetrasodium EDTA, Sodium Sulfate, Methylchloroisothiazolinone, Methylisothiazolinone, Red 40 (CI 16035), Yellow 5 (CI 19140), Red 33 (CI 17200)

Questions or comments?

OTC - QUESTIONS SECTION

1-800-925-4733

Label Copy

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of the label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
1046593	benzalkonium chloride 0.13 % Medicated Liquid Soap	PSN	3
1046593	benzalkonium chloride 1.3 MG/ML Medicated Liquid Soap	SCD	3
1046593	benzalkonium chloride 0.13 % Medicated Liquid Soap	SY	3
1046593	benzalkonium chloride 1.33 MG/ML Medicated Liquid Soap	SY	3

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
362d7abb-94e6-4c60-9a58-266894157713	Product name	1	20231023

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
0363-7211-56	2024-01-30	C162847	48780-1	ba0f9c33-58bc-a910-e053-dadaa90a0b85	0363-7211, Walgreens
0363-7211-56	2022-09-12	C162847	48780-1	ba0f9c33-58bc-a910-e053-dadaa90a0b85	0363-7211, Walgreens
0363-7211-56	2021-01-29	C162847	48780-1	ba0f9c33-58bc-a910-e053-dadaa90a0b85	0363-7211, Walgreens

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
0363-7211-56	WalgreensANTIBACTERIAL HAND REFILL	1650 mL in 1 BOTTLE, PLASTIC	LIQUID	1650		3

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
0363-7211	WALGREENS ANTIBACTERIAL HAND REFILL (BENZALKONIUM CHLORIDE) LIQUID [WALGREEN COMPANY]	3	Legacy NDC, 1 package rows	20220913_54f9feac-f302-4000-8a43-27cc4fdebb4f.zip

Products#

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

DailyMed product names page 1 of 1 · 18 matching rows.

Walgreens ANTIBACTERIAL HAND REFILL
BENZALKONIUM CHLORIDE
WATER
CETRIMONIUM CHLORIDE
GLYCERIN
LAURAMIDOPROPYLAMINE OXIDE
COCO MONOETHANOLAMIDE
SODIUM CHLORIDE
PEG-120 METHYL GLUCOSE DIOLEATE
CITRIC ACID MONOHYDRATE
EDETATE SODIUM
SODIUM SULFATE
METHYLCHLOROISOTHIAZOLINONE
METHYLISOTHIAZOLINONE
FD&C RED NO. 40
FD&C YELLOW NO. 5
D&C RED NO. 33
BENZALKONIUM

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
0363-7211	0363-7211-56

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 16 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
WATER	059QF0KO0R	IACT
CETRIMONIUM CHLORIDE	UC9PE95IBP	IACT
GLYCERIN	PDC6A3C0OX	IACT
LAURAMIDOPROPYLAMINE OXIDE	I6KX160QTV	IACT
COCO MONOETHANOLAMIDE	C80684146D	IACT
SODIUM CHLORIDE	451W47IQ8X	IACT
PEG-120 METHYL GLUCOSE DIOLEATE	YM0K64F20V	IACT
CITRIC ACID MONOHYDRATE	2968PHW8QP	IACT
EDETATE SODIUM	MP1J8420LU	IACT
SODIUM SULFATE	0YPR65R21J	IACT
METHYLCHLOROISOTHIAZOLINONE	DEL7T5QRPN	IACT
METHYLISOTHIAZOLINONE	229D0E1QFA	IACT
FD&C RED NO. 40	WZB9127XOA	IACT
FD&C YELLOW NO. 5	I753WB2F1M	IACT
D&C RED NO. 33	9DBA0SBB0L	IACT
BENZALKONIUM CHLORIDE	F5UM2KM3W7	ACTIB

Source Document#

Source XML · Source PDF

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
e87ed76f-5ab1-9cc4-e053-2a95a90ada21			54f9feac-f302-4000-8a43-27cc4fdebb4f	2022-09-12	Warnings	Exact identifier spl id: e87ed76f-5ab1-9cc4-e053-2a95a90ada21 spl set id: 54f9feac-f302-4000-8a43-27cc4fdebb4f

Reported adverse events (FAERS/openFDA)#

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