WET WIPES TEN- benzalkonium chloride cloth

Wet wipes by

Drug Labeling and Warnings

Wet wipes by is a Otc medication manufactured, distributed, or labeled by TAHA KIMYA KOZMETIK VE TUKETIM URUNLERI SANAYI PAZARLAMA ANONIM SIRKETI. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Benzalkonium Chloride 0.13% w/w. Purpose: Antibacteria

Purpose

Antibacterial

WHEN USING

decreases bacteria on skin

Do not use

• in children less than 2 months of age
• on open skin

STOP USE

Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

Do not expose to direct sunlight, preferably place them in a cool place. Do not use on furniture. Do not flush down toilets. dispose in trash receptacles.

Remove lid and open the seal. Pull up the conrer of the center sheet, twist it and thread through the dispenser split in the lid. Pull sheet out at an angle. When finished close lid flap to retain moisture.

Directions

Peel back flap on front to pull out a wipe.

Unfold and wipe hands thoroughly.

Reseal and let hands dry.

No need to rinse.

Warnings

For external use only. Flammable. Keep away from heat or flame

• Do not replace wipes used for medical procedures.
• These wipes are meant for general cleansing.

Other information

Store between 15-30℃ (59-86℉)

Inactive ingredients

water, phenoxyethanol, propylene glycol, polysorbate 20, peg-7 glyceryl cocoate, cocamidopropyl betaine, parfum, tocopheryl acetate, ethylhexylglycerin, aloe barbadensis leaf extract, disodium edta, citric acid, citronellol, hexyl cinnamal, limonene, linalool.

Package label. Principal display panel

INGREDIENTS AND APPEARANCE

WET WIPES  TEN
benzalkonium chloride cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 78564-006
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.13 mg  in 100

Inactive Ingredients
Ingredient Name	Strength
EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
.BETA.-CITRONELLOL, (R)- (UNII: P01OUT964K)
GLYCERIN (UNII: PDC6A3C0OX)
PEG-7 GLYCERYL COCOATE (UNII: VNX7251543)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
POLYSORBATE 20 (UNII: 7T1F30V5YH)
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
.ALPHA.-HEXYLCINNAMALDEHYDE (UNII: 7X6O37OK2I)
LIMONENE, (+)- (UNII: GFD7C86Q1W)
WATER (UNII: 059QF0KO0R)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
LINALOOL, (+/-)- (UNII: D81QY6I88E)
PHENOXYETHANOL (UNII: HIE492ZZ3T)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 78564-006-10	100 in 1 POUCH; Type 0: Not a Combination Product	06/01/2023

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	06/01/2023

Labeler - TAHA KIMYA KOZMETIK VE TUKETIM URUNLERI SANAYI PAZARLAMA ANONIM SIRKETI (565657236)