Visibly Clean Antibacterial Wet Wipes Fresh Lemonade

Visibly Clean Antibacterial Wet Wipes Fresh Lemonade by

Drug Labeling and Warnings

Visibly Clean Antibacterial Wet Wipes Fresh Lemonade by is a Otc medication manufactured, distributed, or labeled by Flex Beauty Labs LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

VISIBLY CLEAN ANTIBACTERIAL WET WIPES FRESH LEMONADE- benzalkonium chloride cloth 
Flex Beauty Labs LLC

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Visibly Clean Antibacterial Wet Wipes Fresh Lemonade

DRUG FACTS

Active Ingredients

Benzalkonium chloride 0.13%

Purpose

Antibacterial

Use 

to reduce bacteria on the skin.

Warnings

For external use only.

DO NOT USE

if you are allergic to any of the ingredients.

When using this product

do not use in or near eyes. In case of contact, rinse eyes thoroughly with water.

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 years of age: Apply to hands. Allow to dry without wiping. Children under 2 years of age: ask doctor prior to use.

Other information:

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

Inactive Ingredients:

Water (Aqua), Glycerin, Phenoxyethanol, Polysorbate 20, Sodium PCA, Fragrance (Parfum), Ethylhexylglycerin, Tocopheryl Acetate (Vitamin E), Aloe Barbadensis Leaf Extract, Tetrasodium EDTA, Citric Acid.

Question or comments?

info@flexbeautylabs.com 

Distributed by: Flex Beauty Labs, LLC

Orlando, FL, USA

MADE IN TURKEY

Package Labeling:

VISIBLY CLEAN ANTIBACTERIAL WET WIPES FRESH LEMONADE 
benzalkonium chloride cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 72308-038
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	1.3 mg  in 1 g

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
POLYSORBATE 20 (UNII: 7T1F30V5YH)
SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
EDETATE SODIUM (UNII: MP1J8420LU)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 72308-038-00	80 in 1 PACKET	09/15/2020	10/31/2022
1		3.2 g in 1 PATCH; Type 2: Prefilled Drug Delivery Device/System (syringe, patch, etc.)

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	09/15/2020	10/31/2022

Labeler - Flex Beauty Labs LLC (080858917)

Revised: 5/2024

Document Id: 19c1a4af-4e7f-72bb-e063-6394a90aa61e

34390-5

Set id: 3445c60a-0d5b-4190-b5be-1ecd273aab84

Version: 3

Effective Time: 20240531