WET WIPES- benzalkonium chloride swab

Wet Wipes by

Drug Labeling and Warnings

Wet Wipes by is a Otc medication manufactured, distributed, or labeled by HANGZHOU BRIGHT DAILY CHEMICAL 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.

Do not use

over large areas of the body

if you are allergic to any of the ingredients

when using this product,avoid contact with eyes and face.

If contact occurs,flush thoroughly with water.

Stop use and ask a doctor if 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 aPoisonControlCenter right away.

Directions

Foradults 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,trithanolamine ,glycerin,tocopheryl acetate

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

WET WIPES 
benzalkonium chloride swab

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 71198-001
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)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
DISODIUM EDTA-COPPER (UNII: 6V475AX06U)
COPPER TRIETHANOLAMINE (UNII: YBM44X0B6H)
GLYCERIN (UNII: PDC6A3C0OX)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 71198-001-01	10 in 1 PACKAGE	02/13/2017
1		0.042 g in 1 POUCH; Type 0: Not a Combination Product
2	NDC: 71198-001-02	15 in 1 PACKAGE	02/13/2017
2		0.06 g in 1 POUCH; Type 0: Not a Combination Product
3	NDC: 71198-001-03	30 in 1 PACKAGE	02/13/2017
3		0.126 g in 1 POUCH; Type 0: Not a Combination Product
4	NDC: 71198-001-05	80 in 1 PACKAGE	02/13/2017
4		0.336 g in 1 POUCH; Type 0: Not a Combination Product
5	NDC: 71198-001-04	50 in 1 PACKAGE	02/13/2017
5		0.21 g in 1 POUCH; Type 0: Not a Combination Product
6	NDC: 71198-001-06	100 in 1 PACKAGE	02/13/2017
6		0.42 g in 1 POUCH; Type 0: Not a Combination Product
7	NDC: 71198-001-07	1200 in 1 PACKAGE	02/13/2017
7		5.04 g in 1 POUCH; Type 0: Not a Combination Product
8	NDC: 71198-001-08	50 in 1 BOTTLE	02/13/2017
8		0.21 g in 1 POUCH; Type 0: Not a Combination Product
9	NDC: 71198-001-09	80 in 1 BOTTLE	02/13/2017
9		0.336 g in 1 POUCH; Type 0: Not a Combination Product
10	NDC: 71198-001-10	100 in 1 BOTTLE	02/13/2017
10		0.42 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	part333A	02/13/2017

Labeler - HANGZHOU BRIGHT DAILY CHEMICAL CO.,LTD (543255067)

Establishment
Name	Address	ID/FEI	Business Operations
HANGZHOU BRIGHT DAILY CHEMICAL CO.,LTD		543255067	manufacture(71198-001)