SANI LUXE HAND SANITIZER WITH ALCOHOL- alcohol gel 
Celeste Industries Corporation

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Sani Luxe ® Hand Sanitizer Gel with Alcohol

Drug Facts

Active ingredient

Ethyl Alcohol 62.5%

Purpose

Antimicrobial

Uses

Warnings

  • Stop use and ask a doctor if irritation or redness develops, or if condition persists for more than 72 hours.

  • When using this product, avoid contact with eyes. In case of eye contact, flush eyes with water.
  • If swallowed, get medical help or contact a Poison Control Center right away.

  • Keep out of reach of children.

Directions

Other information

Inactive ingredients

Aqua, PEG-4 Diheptanoate, Acrylates/C10-30 Alkyl Acrylate crosspolymer, Fragrance, Aminomethyl Propanol

May contain hydroxypropylcellulose.

284 ml Bottle Label

Sani Luxe ®

HAND SANITIZER GEL

with Alcohol

Kills 99%

of germs

on contact

Caution: Use on hands only.

284ml e

PRINCIPAL DISPLAY PANEL - 284 ml Bottle Label

SANI LUXE HAND SANITIZER WITH ALCOHOL 
alcohol gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71489-007
Route of AdministrationCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL0.625 mL  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
PEG-4 DIHEPTANOATE (UNII: 2DQ7O61VHJ)  
CARBOMER COPOLYMER TYPE A (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 71DD5V995L)  
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)  
HYDROXYPROPYL CELLULOSE, UNSPECIFIED (UNII: 9XZ8H6N6OH)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:71489-007-01284 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product01/24/2019
2NDC:71489-007-02177 mL in 1 BOTTLE; Type 0: Not a Combination Product03/25/202011/14/2022
3NDC:71489-007-0359 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product03/25/2020
4NDC:71489-007-04237 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product05/20/202011/14/2022
5NDC:71489-007-05355 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product03/25/202011/14/2022
6NDC:71489-007-063785 mL in 1 BOTTLE; Type 0: Not a Combination Product03/25/202011/14/2022
7NDC:71489-007-0759 mL in 1 BOTTLE; Type 0: Not a Combination Product06/25/2020
8NDC:71489-007-08177 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product06/25/202011/14/2022
9NDC:71489-007-09237 mL in 1 BOTTLE; Type 0: Not a Combination Product06/25/202011/14/2022
10NDC:71489-007-10284 mL in 1 BOTTLE; Type 0: Not a Combination Product06/25/2020
11NDC:71489-007-11355 mL in 1 BOTTLE; Type 0: Not a Combination Product06/25/202011/14/2022
12NDC:71489-007-123785 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product06/25/202011/14/2022
13NDC:71489-007-13946 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product06/30/2020
14NDC:71489-007-14946 mL in 1 BOTTLE; Type 0: Not a Combination Product06/30/2020
15NDC:71489-007-15530 mL in 1 BOTTLE; Type 0: Not a Combination Product10/14/2020
16NDC:71489-007-16530 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)01/24/2019
Labeler - Celeste Industries Corporation (047795034)

Revised: 12/2023
Document Id: 0c416b47-9c14-d2c5-e063-6394a90aaeae
Set id: 1a259dcf-4d82-4a42-be1f-0e557e0940bd
Version: 12
Effective Time: 20231211
 
Celeste Industries Corporation