Daily Care Antibacterial Wet Hand

Manufacturer: 1 Source Trading LLC
Effective date: 2020-06-27
Label type: HUMAN OTC DRUG LABEL
Version: 2
Source: full-release
Hydrated at: 2026-05-31 23:19:19

Label at a glance#

ProductDaily Care Antibacterial Wet Hand

Active ingredientBENZALKONIUM CHLORIDE

Label structure6 sections

Dosage and administration

Adults and children over 2 years of age: apply to hands, allow to dry without wiping. Children under 2 years of age: ask doctor before use.

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium chloride 0.115%

PURPOSE

OTC - PURPOSE SECTION

Antiseptic

USE:

INDICATIONS & USAGE SECTION

decreases bacteria on skin

WARNINGS:

WARNINGS SECTION

For external use only.

DO NOT USE

OTC - DO NOT USE SECTION

if you are allergic to any of the ingredients.

When using this product

OTC - WHEN USING SECTION

do not get into eyes. If contact occurs, rinse thoroughly with water.

Stop use and ask a doctor if

OTC - STOP USE SECTION

irritation or rash develops and continues 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 immediately.

DIRECTIONS:

DOSAGE & ADMINISTRATION SECTION

Adults and children over 2 years of age: apply to hands, allow to dry without wiping. Children under 2 years of age: ask doctor before use.

INACTIVE INGREDIENTS:

INACTIVE INGREDIENT SECTION

Propylene Glycol,Ethylenediaminetetraacetic acid tetrasodium salt, Sorbitol,Aloe Extract,Glycerine, Purified Water,Fragrance.

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

123

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
1049374	benzalkonium Cl 0.115 % Medicated Pad	PSN	2
1049374	benzalkonium chloride 1.15 MG/ML Medicated Pad	SCD	2
1049374	benzalkonium chloride 0.115 % Medicated Pad	SY	2

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
78107-000-04	2022-01-28	C162847	48780-1	d6a99b39-8f82-a426-e053-dadaa90af4c2	Daily Care Antibacterial Wet Wipes Hand Wipes

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
78107-000-04	Daily Care Antibacterial Wet Hand	40 in 1 BAG	CLOTH	40		2
78107-000-04	Daily Care Antibacterial Wet Hand	0.115 g in 1 PATCH	CLOTH	0.115		2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
78107-000	DAILY CARE ANTIBACTERIAL WET HAND (BENZALKONIUM CHLORIDE) CLOTH [1 SOURCE TRADING LLC]	2	Legacy NDC, 2 package rows	20200628_a759fd99-b00e-00e5-e053-2995a90acb71.zip

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

Daily Care Antibacterial Wet Hand
BENZALKONIUM CHLORIDE
PROPYLENE GLYCOL
SORBITOL
ALOE
GLYCERIN
WATER
BENZALKONIUM

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
78107-000	78107-000-04

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
PROPYLENE GLYCOL	6DC9Q167V3	IACT
SORBITOL	506T60A25R	IACT
ALOE	V5VD430YW9	IACT
GLYCERIN	PDC6A3C0OX	IACT
WATER	059QF0KO0R	IACT
BENZALKONIUM CHLORIDE	F5UM2KM3W7	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
a91a872c-c2d8-1db7-e053-2a95a90a65be			a759fd99-b00e-00e5-e053-2995a90acb71	2020-06-27	Warnings	Exact identifier spl id: a91a872c-c2d8-1db7-e053-2a95a90a65be spl set id: a759fd99-b00e-00e5-e053-2995a90acb71

Reported adverse events (FAERS/openFDA)#

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