XTRACARE WET WIPES- benzethonium chloride swab

XtraCare Wet Wipes by

Drug Labeling and Warnings

XtraCare 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

hand sanitizer to reduce bacteria on the skin.

KEEP OUT OF REACH OF CHILDREN

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

INDICATIONS & USAGE

XtraCare Wet Wipes

Antibacterial

Fresh Citrus Scent

Pocket Size

Kills 99.9% of Germs

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 eye contact occurs, rinse thoroughly with water.

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

DOSAGE & ADMINISTRATION

Directions

for adults and children 2 years and older

• apply to hands
• allow to dry without wiping
• ask a doctor before using on children under 2 years

INACTIVE INGREDIENT

Inactive Ingredients

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

OTHER SAFETY INFORMATION

Questions/comments? 1-855-345-5575

DISTRIBUTED BY

REJOICE INTERNATIONAL INC

NORTHVILLE, MI 48168 USA

MADE IN CHINA

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

XTRACARE WET WIPES 
benzethonium chloride swab

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 58503-062
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZETHONIUM CHLORIDE (UNII: PH41D05744) (BENZETHONIUM - UNII:1VU15B70BP)	BENZETHONIUM CHLORIDE	3 mg  in 100 mg

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: 58503-062-01	18 in 1 PACKAGE	03/13/2014
1		100 mg in 1 APPLICATOR; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	03/13/2014

Labeler - China Ningbo Shangge Cosmetic Technology Corp (529287434)

Establishment
Name	Address	ID/FEI	Business Operations
China Ningbo Shangge Cosmetic Technology Corp		529287434	manufacture(58503-062)