CARROLL ULTREX ANTIMICROBIAL WIPES- benzalkonium chloride cloth

Carroll Ultrex Antimicrobial Wipes by

Drug Labeling and Warnings

Carroll Ultrex Antimicrobial Wipes by is a Otc medication manufactured, distributed, or labeled by Carroll Company. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Drug Facts

Active ingredient

Benzalkonium chloride 0.13% w/w

Purpose

Antimicrobial

Uses

• for hand cleaning to decrease bacteria on the skin
• kills 99.9% of most common germs

Warnings

For external use only

When using this product

• do not use in or near eyes
• discontinue use if irritation and redness develop

Keep out of reach of children. In case of accidental ingestion, seek medical attention or contact a poison control center immediately.

Directions

• Use textured side of wipe to clean hands
• wet hands thoroughly with product
• allow to dry without rinsing

Other information

• store at room temperature

Inactive ingredients

Water, 2-Phenoxyethanol, Alkylpolyglucoside, C 8-10,C10-16, Fragrance, Lauramine,N,N-dimethyl, N-oxide, Tocopherol acetate, Aloe barbadensis leaf juice, PEG-40 Lanolin, Tetrasodium EDTA, Methylchloroisothiazoline, Methylisothiazoline.

SPL UNCLASSIFIED SECTION

Manufactured in the U.S.A. by:
CARROLL ® COMPANY
2900 W. Kingsley Rd., Garland, Texas 75041

PRINCIPAL DISPLAY PANEL - 70 Cloth Canister Label WIPES CARROLL® ULTREX Antimicrobial Wipes -Kills 99.9% of common germs -Contains Aloe and Vitamin E -Moisturizes and conditions skin -Alcohol free CITRUS SCENTED Dual Textured Wipe KEEP OUT OF REACH OF CHILDREN WARNING For external use only. Contains 70 12" x 10" Pre-Moistened Wipes ITEM # 681

INGREDIENTS AND APPEARANCE

CARROLL ULTREX ANTIMICROBIAL WIPES 
benzalkonium chloride cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 10685-681
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.01417 g

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
DECYL GLUCOSIDE (UNII: Z17H97EA6Y)
LAURAMINE OXIDE (UNII: 4F6FC4MI8W)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
EDETATE SODIUM (UNII: MP1J8420LU)
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 10685-681-97	70 in 1 CANISTER; Type 0: Not a Combination Product	09/15/2012

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	09/15/2012

Labeler - Carroll Company (007372329)

Registrant - Carroll Company (007372329)

Establishment
Name	Address	ID/FEI	Business Operations
Carroll Company		007372329	manufacture(10685-681)