LIVEGREEN EUCALYPTUS MINT ANTIBACTERIAL FOAMING HAND WASH- benzalkonium chloride solution

livegreen Eucalyptus Mint ANTIBACTERIAL FOAMING HAND WASH by

Drug Labeling and Warnings

livegreen Eucalyptus Mint ANTIBACTERIAL FOAMING HAND WASH by is a Otc medication manufactured, distributed, or labeled by ENCHANTE ACCESSORIES INC., Xiamen Chengda Industrial Co., Ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Benzalkonium Chloride 0.13%

Purpose

Antibacterial

Use

■ To decrease bacteria on hands

WARNINGS

For external use only

Do not use if you are allergic to any ingredients listed

Discontinue use if irritation or redness occur. Consult a doctor if condition lasts for more than 72 hours

Do not get into eyes. Rinse thoroughly with water if contact occurs

keep out of reach of children

Keep out of reach of children

Directions

Pump soap into dry hands. Lather for at least 20 seconds and rinse thoroughly

Inactive ingredients

Water, Cocamidopropyl Betaine, DMDM Hydantoin, Fragrance, Disodium EDTA, Citric Acid, Eucalyptus Globulus Leaf Extract, Mentha Arvensis
Extract, Yellow 5, Blue 1

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

LIVEGREEN EUCALYPTUS MINT ANTIBACTERIAL FOAMING HAND WASH 
benzalkonium chloride solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 50563-233
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.13 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
DMDM HYDANTOIN (UNII: BYR0546TOW)
DISODIUM HEDTA (UNII: KME849MC7A)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
EUCALYPTUS GLOBULUS LEAF (UNII: S546YLW6E6)
WATER (UNII: 059QF0KO0R)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
MENTHA ARVENSIS WHOLE (UNII: 46477RRB3O)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 50563-233-01	500 mL in 1 BOTTLE; Type 0: Not a Combination Product	06/30/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	06/30/2020

Labeler - ENCHANTE ACCESSORIES INC. (186050696)

Establishment
Name	Address	ID/FEI	Business Operations
Xiamen Chengda Industrial Co., Ltd		540042034	manufacture(50563-233)