Antiseptic Wipes

Manufacturer: Flex Beauty Labs
Effective date: 2020-08-04
Label type: HUMAN OTC DRUG LABEL
Version: 2
Source: full-release
Hydrated at: 2026-05-31 23:23:43

Label at a glance#

ProductAntiseptic Wipes

Active ingredientBENZALKONIUM CHLORIDE

Label structure12 sections

Dosage and administration

Adults and children over 2 yeas of age:Apply to hands. Allow to dry without wioing. Children under 2 year of age:ask doctor prior to use

Label contents#

Full prescribing information#

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Benalkonium chloride (0.115%)

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

Use to reduce bacteria on the skin

Warnings

WARNINGS SECTION

For external use only

Do Not Use

OTC - DO NOT USE SECTION

Do not use if you are allegic to any of the ingredients.

When using this product

OTC - WHEN USING SECTION

When using this product do not use in or near eyes.

In cases of contact, rinse eyes thoroughly with water.

Stop use and ask a doctor if

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or redness develops.

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

Adults and children over 2 yeas of age:Apply to hands. Allow to dry without wioing.
Children under 2 year of age:ask doctor prior to use

Other information

OTHER SAFETY INFORMATION

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

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Glycerin, Aloe barbadensis leaf juice, Fragrance, 4Na EDTA,Propylene Glycol. sorbito

principal display panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

wipes3wipes2wipes1

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
72308-028-20	2022-01-28	C162847	48780-1	d6a99b39-447c-a426-e053-dadaa90af4c2	Germout- Wet Wipes Antibaterial
72308-028-40	2022-01-28	C162847	48780-1	d6a99b39-447c-a426-e053-dadaa90af4c2	Germout- Wet Wipes Antibaterial
72308-028-80	2022-01-28	C162847	48780-1	d6a99b39-447c-a426-e053-dadaa90af4c2	Germout- Wet Wipes Antibaterial

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
72308-028-20	Antiseptic Wipes	20 in 1 PACKAGE	CLOTH	20	2
72308-028-20	Antiseptic Wipes	1 mg in 1 PACKET	CLOTH	1	2
72308-028-40	Antiseptic Wipes	1 mg in 1 PACKET	CLOTH	1	2
72308-028-40	Antiseptic Wipes	40 in 1 PACKAGE	CLOTH	40	2
72308-028-80	Antiseptic Wipes	80 in 1 PACKAGE	CLOTH	80	2
72308-028-80	Antiseptic Wipes	1 mg in 1 PACKET	CLOTH	1	2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
72308-028	ANTISEPTIC WIPES (BENZALKONIUM CHLORIDE (0.115%)) CLOTH [FLEX BEAUTY LABS]	2	Legacy NDC, 6 package rows	20200805_7d7b42b4-df85-4995-be55-6611526993f8.zip

Products#

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

DailyMed product names page 1 of 1 · 11 matching rows.

Antiseptic Wipes
Benzalkonium Chloride (0.115%)
WATER
GLYCERIN
PROPYLENE GLYCOL
ALOE VERA LEAF
SORBITOL
EDETATE SODIUM
ETHYLHEXYLGLYCERIN
BENZALKONIUM CHLORIDE
BENZALKONIUM

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
72308-028	72308-028-20, 72308-028-40, 72308-028-80

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
WATER	059QF0KO0R	IACT
GLYCERIN	PDC6A3C0OX	IACT
PROPYLENE GLYCOL	6DC9Q167V3	IACT
ALOE VERA LEAF	ZY81Z83H0X	IACT
SORBITOL	506T60A25R	IACT
EDETATE SODIUM	MP1J8420LU	IACT
ETHYLHEXYLGLYCERIN	147D247K3P	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
ac0daaf1-be48-f6e3-e053-2995a90ad683			7d7b42b4-df85-4995-be55-6611526993f8	2020-08-04	Warnings	Exact identifier spl id: ac0daaf1-be48-f6e3-e053-2995a90ad683 spl set id: 7d7b42b4-df85-4995-be55-6611526993f8

Reported adverse events (FAERS/openFDA)#

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