ANTIBACTERIAL MOIST WIPES- benzalkonium chloride swab

Antibacterial Moist Wipes by

Drug Labeling and Warnings

Antibacterial Moist Wipes by is a Otc medication manufactured, distributed, or labeled by JIANGSU TERRA MEDICAL TECHNOLOGY CO LTD. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Benzalkonium chloride  0.1%

Purpose

antibacterial

Use

decreases bacteria on skin

Warnings

for external use only

over large areas of the body 

if you are allergic to ay of the ingredients

When using this product avoid contact with eyes and face.

if contact occurs,flush throughly with water

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

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

for adults and children of 2 years and over.

children under 2 years ask a doctor before use

allow to dry without wiping

INACTIVE INGREDIENT

water ,sodium lauryl sulfate,fragrance,2-bromo-2-nitropropane-1,3-diol,aloe barbadensis leaf extract,disodium EDTA,triethanolamine,glycerin,tocopheryl acetate.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

ANTIBACTERIAL MOIST WIPES 
benzalkonium chloride swab

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69733-558
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.1 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
SODIUM LAURYL SULFATE (UNII: 368GB5141J)
2-BROMO-2-NITROETHANOL (UNII: FA22WV2B2Z)
2-METHYL-2-PROPYLPROPANE-1,3-DIOL (UNII: YLM5KRU0P4)
ALOE ARBORESCENS LEAF (UNII: 09TD8L5SQV)
DISODIUM EDTA-COPPER (UNII: 6V475AX06U)
TRIETHANOLAMINE BENZOATE (UNII: M3EN4GC19W)
GLYCERIN (UNII: PDC6A3C0OX)
TOCOPHERYL RETINOATE (UNII: 0WN694NBMM)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 69733-558-02	20 in 1 PACKAGE
1		0.00297 g in 1 POUCH; 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	04/15/2015

Labeler - JIANGSU TERRA MEDICAL TECHNOLOGY CO LTD (421340473)

Establishment
Name	Address	ID/FEI	Business Operations
JIANGSU TERRA MEDICAL TECHNOLOGY CO LTD		421340473	manufacture(69733-558)