Label: SIGNATURE SERIES ENRICHED FOAM ALCOHOL HAND SANITIZER- alcohol liquid

  • Category: HUMAN OTC DRUG LABEL

Drug Label Information

Updated December 18, 2023

If you are a healthcare professional or from the pharmaceutical industry please visit this version.

View All Sections
  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • Active Ingredient

    Alcohol Denat. 75% (v/v)

  • Purpose

    Antiseptic cleanser

  • Use

    To decrease potentially harmful germs on skin.

  • Warnings

    • Flammable. Keep away from fire or flame.
    • For external use only.

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

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

    • Keep out of reach of children.
    • If swallowed, do not induce vomiting, get medical attention.

    Read material safety data sheet before using product

  • Directions

    • Apply generously to hands. Rub hands together. Allow hands to dry. Repeat daily as necessary.
  • Inactive Ingredients

    Water (Aqua), PEG-6 Caprylic Glycerides, Sodium Lactate, PEG-14M, Silica, Disodium Lauriminodipropionate Tocopheryl Phosphates, Phenoxyethanol, Benzoic Acid, Dehydroacetic Acid, PEG/PPG-25/25 Dimethicone, Shea Butteramidopropyl Betaine, Hexylene Glycol, Sodium Citrate, Lactic Acid

  • Questions?

    1-800-347-9800 Mon.–Fri., 8 AM–5 PM EST.

  • PRINCIPAL DISPLAY PANEL - 500 mL Pouch Box

    Rubbermaid®
    Commercial Products

    Enriched Foam Alcohol Hand Sanitizer

    500 mL (16.9 FL. OZ. U.S.)

    HAND SANITIZER

    CiNTAS®
    Signature Series®

    PRINCIPAL DISPLAY PANEL - 500 mL Pouch Box
  • INGREDIENTS AND APPEARANCE
    SIGNATURE SERIES ENRICHED FOAM ALCOHOL HAND SANITIZER 
    alcohol liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:42961-017
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL75 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    CAPRYLOCAPROYL POLYOXYLGLYCERIDES 6 (UNII: GO50W2HWO8)  
    SODIUM LACTATE (UNII: TU7HW0W0QT)  
    POLYETHYLENE OXIDE 600000 (UNII: 2126FD486L)  
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
    DISODIUM LAURIMINODIPROPIONATE TOCOPHERYL PHOSPHATES (UNII: 0K5Y9U1P6M)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    BENZOIC ACID (UNII: 8SKN0B0MIM)  
    DEHYDROACETIC ACID (UNII: 2KAG279R6R)  
    PEG/PPG-25/25 DIMETHICONE (UNII: ND6MYD0T84)  
    HEXYLENE GLYCOL (UNII: KEH0A3F75J)  
    SODIUM CITRATE, UNSPECIFIED FORM (UNII: 1Q73Q2JULR)  
    LACTIC ACID, UNSPECIFIED FORM (UNII: 33X04XA5AT)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:42961-017-014 in 1 BOX05/08/2020
    1500 mL in 1 POUCH; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC MONOGRAPH DRUGM00405/08/2020
    Labeler - Cintas Corporation (056481716)
    Registrant - Rubbermaid Commercial Products LLC (049924368)
    Establishment
    NameAddressID/FEIBusiness Operations
    NWL Netherlands Services B.V.494692088MANUFACTURE(42961-017)
View All Sections

Find additional resources

(also available in the left menu)

Safety

Report Adverse Events, FDA Safety Recalls, Presence in Breast Milk

Related Resources

Medline Plus, Clinical Trials

More Info on this Drug

Get Label RSS Feed, View NDC Code(s)NEW!