SANILUXE HAND SANITIZER ALCOHOL FREE- benzalkonium chloride gel 
Celeste Industries Corporation

----------

SaniLuxe™ Hand Sanitizer Gel Alcohol Free

Drug Facts

Active ingredient

Benzalkonium Chloride 0.1%

Purpose

Antimicrobial

Uses

Warnings

  • Keep out of reach of children.

  • When using this product avoid contact with eyes. In case of eye contact, flush eyes with water.

  • Stop use and ask a doctor if irritation or redness develops, or if condition persists for more than 72 hours.
  • If swallowed, get medical help or contact a Poison Control Center right away.

Directions

Inactive ingredients

Water (Aqua), Triethylene Glycol, Glycereth-26, Cocamidopropyl PG-Dimonium Cloride Phosphate,Hydroxyethylcellulose, DMDM Hydantoin, Triethanolamine, Fragrance (Aroma), Iodopropynyl Butyl Carbamate, 1, 3-Butanediol

284 ml Bottle Label

SaniLuxe™

HAND SANITIZER GEL

Alcohol free

Kills 99%

of germs

on contact

Caution: Use on hands only.

284ml e

PRINCIPAL DISPLAY PANEL - 284 ml Bottle Label

SANILUXE HAND SANITIZER ALCOHOL FREE 
benzalkonium chloride gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71489-008
Route of AdministrationCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE1 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
TRIETHYLENE GLYCOL (UNII: 3P5SU53360)  
GLYCERETH-26 (UNII: NNE56F2N14)  
COCAMIDOPROPYL PROPYLENE GLYCOL-DIMONIUM CHLORIDE PHOSPHATE (UNII: H2KVQ74JM4)  
HYDROXYETHYL CELLULOSE (5000 MPA.S AT 1%) (UNII: X70SE62ZAR)  
DMDM HYDANTOIN (UNII: BYR0546TOW)  
TROLAMINE (UNII: 9O3K93S3TK)  
IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB)  
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:71489-008-01284 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product02/19/2019
2NDC:71489-008-02177 mL in 1 BOTTLE; Type 0: Not a Combination Product06/25/2020
3NDC:71489-008-0359 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product06/25/2020
4NDC:71489-008-04237 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product06/25/2020
5NDC:71489-008-05355 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product06/25/2020
6NDC:71489-008-063785 mL in 1 BOTTLE; Type 0: Not a Combination Product06/25/2020
7NDC:71489-008-0759 mL in 1 BOTTLE; Type 0: Not a Combination Product06/25/2020
8NDC:71489-008-08177 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product06/25/2020
9NDC:71489-008-09237 mL in 1 BOTTLE; Type 0: Not a Combination Product06/25/2020
10NDC:71489-008-10284 mL in 1 BOTTLE; Type 0: Not a Combination Product06/25/2020
11NDC:71489-008-11355 mL in 1 BOTTLE; Type 0: Not a Combination Product06/25/2020
12NDC:71489-008-123785 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product06/25/2020
13NDC:71489-008-13946 mL in 1 BOTTLE; Type 0: Not a Combination Product06/30/2020
14NDC:71489-008-14946 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product06/30/2020
15NDC:71489-008-15530 mL in 1 BOTTLE; Type 0: Not a Combination Product10/14/2020
16NDC:71489-008-16530 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product10/14/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph Drug505G(a)(3)02/19/2019
Labeler - Celeste Industries Corporation (047795034)

Revised: 12/2023
Document Id: 0c416f8c-7ba1-d27a-e063-6394a90ae0d7
Set id: 3e4fde0d-1c65-4fd3-867a-80b46cc53b32
Version: 6
Effective Time: 20231211
 
Celeste Industries Corporation