Wet Ones Antibacterial Hand Wipes Spring Bliss: Package Insert and Label Information

WET ONES ANTIBACTERIAL HAND WIPES SPRING BLISS- benzalkonium chloride swab
Edgewell Personal Care Brands LLC

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Benzalkonium Chloride 0.11%

Purpose

Antibacterial

Use

to decrease bacteria on skin

Warnings

For external use only

Do not use

If you are allergic to any of the ingredients

if irritation and redness develop

When using this prodcut

Keep out of eyes. In case of contact with eyes, flush thoroughly with water.

Stop use and ask a doctor

If condition persists for more than 72 hours

Keep out of reach of children

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

Directions

Adults and children 3 years and over; rub hands thoroughly with product and allow skin to dry without wiping

Children under 3 years: ask a doctor before use

Inactive ingredients

Water, Ethyl Alcohol, Propylene Glycol, Phenoxyethanol, Lauryl Glucoside, Iodopropynyl Butylcarbamate, Tetrasodium EDTA, 2-Bromo-2-Nitropropane-1,3-Diol, Citric Acid, Fragrance, Aloe Barbadensis Leaf Extract, Chamomilla Recutita (Matricaria) Flower Extract

Questions or Comments?

Call 1-866-WET-111S

(1-866-936-1117), M-F

Principal Display Panel

ANTIBACTERIAL

25

wipes

label
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ANTIBACTERIAL

Soft Texture

50

wipes

label2
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Wet

Ones(r)

ANTIBACTERIAL

HAND WIPES

Spring Bliss

Touch of Aloe

label3
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Wet

Ones(r)

ANTIBACTERIAL HAND WIPES

Spring Bliss

Touch of Aloe

label
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WET ONES ANTIBACTERIAL HAND WIPES SPRING BLISS
benzalkonium chloride swab
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:63354-905
Route of Administration TOPICAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
BENZALKONIUM CHLORIDE (BENZALKONIUM) BENZALKONIUM CHLORIDE 0.11 g in 100 g
Inactive Ingredients
Ingredient Name Strength
WATER
PROPYLENE GLYCOL
ALCOHOL
SODIUM HYDROXIDE
PHENOXYETHANOL
ALOE VERA LEAF
CHAMOMILE
POLYETHYLENE GLYCOL, UNSPECIFIED
EDETATE SODIUM
SODIUM BENZOATE
IODOPROPYNYL BUTYLCARBAMATE
POTASSIUM SORBATE
ANHYDROUS CITRIC ACID
BRONOPOL
CITRIC ACID MONOHYDRATE
LAURYL GLUCOSIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:63354-905-25 25 g in 1 POUCH None
2 NDC:63354-905-50 50 g in 1 POUCH None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC monograph not final part333A 07/25/2022
Labeler — Edgewell Personal Care Brands LLC (151179769)

Revised: 07/2022 Edgewell Personal Care Brands LLC

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