LUCKY ALCOHOL FREE HAND SANITIZER VITAMIN E- 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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Lucky Alcohol Free hand sanitizer-Vit E

Active Ingredient

Benzalkonium Chloride 0.13%

Purpose

Antiseptic

Uses

hand sanitizer to help reduce bacteria on the skin that could cause disease

Warnings

For external use only

When using this product

do not get into the eyes. If contact occurs, rinse eyes thoroughly with water.

Stop use and ask a doctor if


if irritation or rash appears and lasts

Keep out of reach of children

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

Directions

■ place enough product in your palm ■ rub hands vigorously until dry ■ children under 6 years of age should be supervised when using this product

Other information

■ store below 106ºF (41ºC) ■ may discolor certain fabrics or surfaces

Inactive ingredients

water, glycerin, carbomer, poly sorbate 20, PEG-40 hydrogenated castor oil, fragrance, sodium hydroxide, methylchloroisothiazolinone, methylisothiazolinone, tocopheryl acetate

Package Label

Package Label

LUCKY ALCOHOL FREE HAND SANITIZER  VITAMIN E
benzalkonium chloride liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:20276-139
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)  
POLYSORBATE 20 (UNII: 7T1F30V5YH)  
SODIUM HYDROXIDE (UNII: 55X04QC32I)  
GLYCERIN (UNII: PDC6A3C0OX)  
POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F)  
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)  
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:20276-139-08236 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product03/10/2020
2NDC:20276-139-10296 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product03/10/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A03/10/2020
Labeler - Delta Brands, Inc (102672008)

Revised: 3/2020
Document Id: a160f27a-6587-070a-e053-2a95a90a15c7
Set id: a161bbe3-9e6b-50c5-e053-2995a90a954a
Version: 1
Effective Time: 20200321
 
Delta Brands, Inc