LUCKY ANTIBACTERIAL- benzalkonium chloride liquid 
Delta Brands, Inc

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Active Ingredient

Benzalkonium Chloride 0.13%

Purpose

Antibacterial

Uses

for hand washing to decrease bacteria on the skin

Warnings

For external use only

When using this product

■ avoid contact with the eyes. In case of eye contact, flush with water.

Stop use and ask a doctor if


■ irritation and redness develops

Keep out of reach of children

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

Directions

■ pump into hands, wet as needed ■ lather vigorously for at least 15 seconds ■ wash skin, rinse thoroughly and dry

Inactive ingredients

water, cocamidopropyl betaine, cetrimonium chloride, coco-glucoside, glyceryl oleate, cocamide MEA, glycerin, PEG-150 distearate, sodium chloride, fragrance, citric acid, methylchloroisothiazolinone, methylisothiazolinone, FDC blue no. 1

Package Label

package label

LUCKY  ANTIBACTERIAL
benzalkonium chloride liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:20276-147
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE0.13 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)  
COCO GLUCOSIDE (UNII: ICS790225B)  
GLYCERYL OLEATE (UNII: 4PC054V79P)  
GLYCERIN (UNII: PDC6A3C0OX)  
CETRIMONIUM CHLORIDE (UNII: UC9PE95IBP)  
COCO MONOETHANOLAMIDE (UNII: C80684146D)  
PEG-150 DISTEARATE (UNII: 6F36Q0I0AC)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)  
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)  
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:20276-147-12400 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product05/10/2016
2NDC:20276-147-75221 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product11/04/2020
3NDC:20276-147-09266 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product11/04/2020
4NDC:20276-147-11333 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product11/04/2020
5NDC:20276-147-14414 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product11/04/2020
6NDC:20276-147-15444 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product11/04/2020
7NDC:20276-147-16500 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product11/04/2020
8NDC:20276-147-401180 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product11/04/2020
9NDC:20276-147-641890 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product11/04/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A05/10/2016
Labeler - Delta Brands, Inc (102672008)

Revised: 1/2021
 
Delta Brands, Inc