LUCKY ANTIBACTERIAL FOAMING HANDWASH- benzalkonium chloride liquid

LUCKY by

Drug Labeling and Warnings

LUCKY by is a Otc medication manufactured, distributed, or labeled by Delta Brands, Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Benzalkonium Chloride 0.13%

Purpose

Antibacterial

Uses

to decrease bacteria on the skin

Warnings

For external use only

■ avoid eye contact. In case of eye contact, flush with water. If irritation occurs discontinue use of product

Keep out of reach of children

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

■ pump into hands, lather vigorously and rinse

Inactive ingredients

water, cocamidopropyl betaine, decyl glucoside, glycerin, fragrance, citric acid, polyquaternium-7, xanthan gum, methylchloroisothiazolinone, methylisothiazolinone, polysorbate-20, tetrasodium EDTA, aloe barbadensis leaf juice, FDC blue no. 1, DC red no. 33

Package Label

INGREDIENTS AND APPEARANCE

LUCKY  ANTIBACTERIAL FOAMING HANDWASH
benzalkonium chloride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 20276-143
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
D&C RED NO. 33 (UNII: 9DBA0SBB0L)
WATER (UNII: 059QF0KO0R)
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
DECYL GLUCOSIDE (UNII: Z17H97EA6Y)
XANTHAN GUM (UNII: TTV12P4NEE)
GLYCERIN (UNII: PDC6A3C0OX)
POLYQUATERNIUM-7 (70/30 ACRYLAMIDE/DADMAC; 1600000 MW) (UNII: 0L414VCS5Y)
POLYSORBATE 20 (UNII: 7T1F30V5YH)
EDETATE SODIUM (UNII: MP1J8420LU)
SODIUM CITRATE (UNII: 1Q73Q2JULR)
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
ALOE VERA LEAF (UNII: ZY81Z83H0X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 20276-143-75	221 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	06/01/2017

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	06/01/2017

Labeler - Delta Brands, Inc (102672008)