Label: SANI LUXE- alcohol cloth

  • NDC Code(s): 71489-009-01
  • Packager: Celeste Industries Corporation
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 11, 2023

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  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • Active Ingredient

    Ethyl alcohol (ethanol) 70%

  • Purpose

    Antimicrobial

  • Uses

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

    For external use only.

    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.

    Keep out of reach of children. If swallowed, get medical help or
    contact a Poison Control Center right away.

  • Directions

    • Apply to hands
    • Allow skin to dry without wiping
  • Inactive Ingredients

    Water, Cocamindopropyl PG-Dimonium, Chloride Phosphate, Linear alcohol ethoxylate, Fragrance.

  • SPL UNCLASSIFIED SECTION

    Expires:
    DDMMMYYYY

    Manufactured by:
    Celeste Industries Corporation
    Easton, Maryland 21601 • USA

  • 1.75 mL

    SaniLuxe® HAND SANITIZER WIPE 1.75 mL Antibacterial Hand Sanitizer Kills 99.9% of germs Open packet Unfold cloth Wipe surfaces Phone • Computer • Communications Equipment • Hands

  • INGREDIENTS AND APPEARANCE
    SANI LUXE 
    alcohol cloth
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71489-009
    Route of AdministrationCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL0.7 mL  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    C9-11 PARETH-6 (UNII: KCE0V8JT7W)  
    COCAMIDOPROPYL PG-DIMONIUM CHLORIDE PHOSPHATE (UNII: H2KVQ74JM4)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:71489-009-011.75 mL in 1 PACKET; Type 0: Not a Combination Product02/05/2021
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)02/05/2021
    Labeler - Celeste Industries Corporation (047795034)
    Establishment
    NameAddressID/FEIBusiness Operations
    Celeste Industries Corporation968381918manufacture(71489-009)
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