Sani Luxe Foaming Hand Sanitizer Alcohol Free

Manufacturer
Celeste Industries Corporation
Effective date
2024-07-08
Label type
HUMAN OTC DRUG LABEL
Version
10
Source
full-release
Hydrated at
2026-06-01 00:14:53

Label at a glance#

ProductSani Luxe Foaming Hand Sanitizer Alcohol Free
Active ingredientBENZALKONIUM CHLORIDE
Label structure8 sections

Indications and uses

Recommended for repeated use For hand sanitizing to decrease bacteria on the skin

Dosage and administration

Pump a small amount of foam into palm of hand Rub hands together briskly until dry Rub thoroughly over all surfaces of both hands

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.1%

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Uses

INDICATIONS & USAGE SECTION

  • Recommended for repeated use
  • For hand sanitizing to decrease bacteria on the skin

Warnings

WARNINGS SECTION

  • For external use only.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

  • Keep out of reach of children.

OTC - WHEN USING SECTION

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

OTC - STOP USE SECTION

  • 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

DOSAGE & ADMINISTRATION SECTION

  • Pump a small amount of foam into palm of hand
  • Rub hands together briskly until dry
  • Rub thoroughly over all surfaces of both hands

Inactive ingredients

INACTIVE INGREDIENT SECTION

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

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

SaniLuxe™

FOAMING HAND SANITIZER

Alcohol free

  • Requires no water or towels.
  • Apply small amount to hands

    and rub until dry.

Kills 99%

of germs

on contact

Caution: Use on hands only.

8 fl oz • 236ml e

PRINCIPAL DISPLAY PANEL - 236 ml Bottle LabelPRINCIPAL DISPLAY PANEL - 236 ml Bottle Label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1038799benzalkonium chloride 0.1 % Topical FoamPSN10
1038799benzalkonium chloride 1 MG/ML Topical FoamSCD10
1038799benzalkonium chloride 0.1 % Topical FoamSY10

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
71489-006-012024-01-30C16284748780-11030e365-2470-111a-e063-dadaa90a10e2SaniLuxe™ Foaming Hand Sanitizer Alcohol Free
71489-006-022024-01-30C16284748780-11030e365-2470-111a-e063-dadaa90a10e2SaniLuxe™ Foaming Hand Sanitizer Alcohol Free
71489-006-032024-01-30C16284748780-11030e365-2470-111a-e063-dadaa90a10e2SaniLuxe™ Foaming Hand Sanitizer Alcohol Free
71489-006-042024-01-30C16284748780-11030e365-2470-111a-e063-dadaa90a10e2SaniLuxe™ Foaming Hand Sanitizer Alcohol Free
71489-006-052024-01-30C16284748780-11030e365-2470-111a-e063-dadaa90a10e2SaniLuxe™ Foaming Hand Sanitizer Alcohol Free
71489-006-062024-01-30C16284748780-11030e365-2470-111a-e063-dadaa90a10e2SaniLuxe™ Foaming Hand Sanitizer Alcohol Free
71489-006-072024-01-30C16284748780-11030e365-2470-111a-e063-dadaa90a10e2SaniLuxe™ Foaming Hand Sanitizer Alcohol Free
71489-006-082024-01-30C16284748780-11030e365-2470-111a-e063-dadaa90a10e2SaniLuxe™ Foaming Hand Sanitizer Alcohol Free
71489-006-092024-01-30C16284748780-11030e365-2470-111a-e063-dadaa90a10e2SaniLuxe™ Foaming Hand Sanitizer Alcohol Free
71489-006-102024-01-30C16284748780-11030e365-2470-111a-e063-dadaa90a10e2SaniLuxe™ Foaming Hand Sanitizer Alcohol Free
71489-006-112024-01-30C16284748780-11030e365-2470-111a-e063-dadaa90a10e2SaniLuxe™ Foaming Hand Sanitizer Alcohol Free
71489-006-122024-01-30C16284748780-11030e365-2470-111a-e063-dadaa90a10e2SaniLuxe™ Foaming Hand Sanitizer Alcohol Free
71489-006-132024-01-30C16284748780-11030e365-2470-111a-e063-dadaa90a10e2SaniLuxe™ Foaming Hand Sanitizer Alcohol Free
71489-006-142024-01-30C16284748780-11030e365-2470-111a-e063-dadaa90a10e2SaniLuxe™ Foaming Hand Sanitizer Alcohol Free
71489-006-152024-01-30C16284748780-11030e365-2470-111a-e063-dadaa90a10e2SaniLuxe™ Foaming Hand Sanitizer Alcohol Free
71489-006-162024-01-30C16284748780-11030e365-2470-111a-e063-dadaa90a10e2SaniLuxe™ Foaming Hand Sanitizer Alcohol Free

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
71489-006-01Sani Luxe Foaming Hand Sanitizer Alcohol Free237 mL in 1 BOTTLE, PUMPLIQUID23710
71489-006-02Sani Luxe Foaming Hand Sanitizer Alcohol Free56 mL in 1 BOTTLE, PUMPLIQUID5610
71489-006-03Sani Luxe Foaming Hand Sanitizer Alcohol Free177 mL in 1 BOTTLELIQUID17710
71489-006-04Sani Luxe Foaming Hand Sanitizer Alcohol Free284 mL in 1 BOTTLE, PUMPLIQUID28410
71489-006-05Sani Luxe Foaming Hand Sanitizer Alcohol Free355 mL in 1 BOTTLE, PUMPLIQUID35510
71489-006-06Sani Luxe Foaming Hand Sanitizer Alcohol Free3785 mL in 1 BOTTLELIQUID378510
71489-006-07Sani Luxe Foaming Hand Sanitizer Alcohol Free59 mL in 1 BOTTLELIQUID5910
71489-006-08Sani Luxe Foaming Hand Sanitizer Alcohol Free177 mL in 1 BOTTLE, PUMPLIQUID17710
71489-006-09Sani Luxe Foaming Hand Sanitizer Alcohol Free237 mL in 1 BOTTLELIQUID23710
71489-006-10Sani Luxe Foaming Hand Sanitizer Alcohol Free284 mL in 1 BOTTLELIQUID28410
71489-006-11Sani Luxe Foaming Hand Sanitizer Alcohol Free355 mL in 1 BOTTLELIQUID35510
71489-006-12Sani Luxe Foaming Hand Sanitizer Alcohol Free3785 mL in 1 BOTTLE, PUMPLIQUID378510
71489-006-13Sani Luxe Foaming Hand Sanitizer Alcohol Free946 mL in 1 BOTTLELIQUID94610
71489-006-14Sani Luxe Foaming Hand Sanitizer Alcohol Free946 mL in 1 BOTTLE, PUMPLIQUID94610
71489-006-15Sani Luxe Foaming Hand Sanitizer Alcohol Free530 mL in 1 BOTTLELIQUID53010
71489-006-16Sani Luxe Foaming Hand Sanitizer Alcohol Free530 mL in 1 BOTTLE, PUMPLIQUID53010

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71489-006SANI LUXE FOAMING HAND SANITIZER ALCOHOL FREE (BENZALKONIUM CHLORIDE) LIQUID [CELESTE INDUSTRIES CORPORATION]10Current NDC, Legacy NDC, 16 package rows20240709_7549428e-b10f-45b9-b414-0c6e8b41c398.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 10 matching rows.

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Sani Luxe Foaming Hand Sanitizer Alcohol FreeBENZALKONIUM CHLORIDECeleste Industries Corporation7549428e-b10f-45b9-b414-0c6e8b41c3982024-07-08WarningsExact identifier
ndc (package): 71489-006-11
ndc (package): 71489-006-08
ndc (package): 71489-006-02
ndc (package): 71489-006-06
ndc (package): 71489-006-09
ndc (package): 71489-006-16
ndc (package): 71489-006-10
ndc (package): 71489-006-04
ndc (package): 71489-006-05
ndc (package): 71489-006-01
ndc (package): 71489-006-12
ndc (package): 71489-006-03
ndc (package): 71489-006-13
ndc (package): 71489-006-07
ndc (package): 71489-006-14
ndc (package): 71489-006-15
ndc (product): 71489-006
ndc11 (package): 71489000606
ndc11 (package): 71489000601
ndc11 (package): 71489000612
ndc11 (package): 71489000605
ndc11 (package): 71489000611
ndc11 (package): 71489000602
ndc11 (package): 71489000616
ndc11 (package): 71489000603
ndc11 (package): 71489000609
ndc11 (package): 71489000607
ndc11 (package): 71489000608
ndc11 (package): 71489000604
ndc11 (package): 71489000610
ndc11 (package): 71489000615
ndc11 (package): 71489000614
ndc11 (package): 71489000613
spl id: 1cbe491e-af31-8dd8-e063-6394a90ae2f5
spl set id: 7549428e-b10f-45b9-b414-0c6e8b41c398

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.