WET WIPES- benzethonium chloride cloth

Wet Wipes by

Drug Labeling and Warnings

Wet Wipes by is a Otc medication manufactured, distributed, or labeled by China Ningbo Shangge Cosmetic Technology Corp. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active Ingredient                                    Purpose

Benzethonium Chloride 0.3% ............... Antibacterial

PURPOSE

Uses

decrease bacteria on skin

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.

INDICATIONS & USAGE

XtraCare Wet Wipes

Antibacterial Hand Wipes

Fresh Scent

Kills 99.9% of germs

Pull up here

Resealable

32 Thick Moist Wipes

14.6 cm x 19 cm

XtraCare Antibacterial Hand Wipes kill 99.9% of germs, helping prevent the spread of bacteria, and they remove dirt, providing a better clean-up after hand sanitizers. They are ideal for quick clean-ups after contact with germs, sticky foods, greasy dirt and everyday messes.

XtraCare Antibacterial Hand Wipes are formulated to be tough on dirt and germs, yet gentle on skin. Help keep your family healthy and clean anytime and anywhere, when soap and water are not available.

WARNINGS

Warnings

For external use only

Do not use if you are allergic to any of the ingredients

When using this product do not get into eyes. If contact occurs, rinse thoroughly with water.

Stop use and ask a doctor if irritation or rash develops and continues for more than 72 hours.

DOSAGE & ADMINISTRATION

Directions

adults and children 2 years and over

• apply to hands
• allow to dry without wiping

children under 2 years

• ask a doctor before use

INACTIVE INGREDIENT

Inactive Ingredients

water, ethyl alcohol, propylene glycol, PEG-40 hydrogenated castor oil, fragrance, disodium EDTA, aloe barbadensis leaf juice, methylparaben, propylparaben.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

WET WIPES 
benzethonium chloride cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 58503-067
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZETHONIUM CHLORIDE (UNII: PH41D05744) (BENZETHONIUM - UNII:1VU15B70BP)	BENZETHONIUM CHLORIDE	0.3 g

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
ALCOHOL (UNII: 3K9958V90M)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F)
EDETATE DISODIUM (UNII: 7FLD91C86K)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
METHYLPARABEN (UNII: A2I8C7HI9T)
PROPYLPARABEN (UNII: Z8IX2SC1OH)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 58503-067-01	32 in 1 PACKAGE; Type 0: Not a Combination Product	12/08/2014

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	12/08/2014

Labeler - China Ningbo Shangge Cosmetic Technology Corp (529287434)

Establishment
Name	Address	ID/FEI	Business Operations
China Ningbo Shangge Cosmetic Technology Corp		529287434	manufacture(58503-067)