ANTISEPTIC WIPES (benzalkonium chloride- 0.115% cloth

Antiseptic Wipes by

Drug Labeling and Warnings

Antiseptic Wipes by is a Otc medication manufactured, distributed, or labeled by Flex Beauty Labs. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredients

Benalkonium chloride (0.115%)

Purpose

Antiseptic

Use

Use to reduce bacteria on the skin

Warnings

For external use only

Do Not Use

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

When using this product 

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

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

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away

Directions:

• 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

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

Inactive ingredients

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

principal display panel

INGREDIENTS AND APPEARANCE

ANTISEPTIC WIPES 
benzalkonium chloride (0.115%) cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 72308-028
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.115 mg  in 100 mg

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
SORBITOL (UNII: 506T60A25R)
EDETATE SODIUM (UNII: MP1J8420LU)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 72308-028-20	20 in 1 PACKAGE	08/03/2020
1		1 mg in 1 PACKET; Type 1: Convenience Kit of Co-Package
2	NDC: 72308-028-40	40 in 1 PACKAGE	08/03/2020
2		1 mg in 1 PACKET; Type 1: Convenience Kit of Co-Package
3	NDC: 72308-028-80	80 in 1 PACKAGE	08/03/2020
3		1 mg in 1 PACKET; Type 1: Convenience Kit of Co-Package

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	06/23/2020

Labeler - Flex Beauty Labs (080858917)