Label: PACIFIC BLUE SELECT GEL HAND SANITIZER FRAGRANCE AND DYE FREE- ethyl alcohol liquid

  • NDC Code(s): 54622-308-01
  • Packager: Georgia-Pacific Consumer Products
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph not final

DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Label Information

Updated December 31, 2019

If you are a consumer or patient please visit this version.

  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • Active ingredient

    Ethyl alcohol, 67% v/v

  • Purpose

    Antiseptic

  • Uses

    • To decrease bacteria on skin that could cause disease
    • Recommended for repeated use

  • Warnings

    • FLAMMABLE, keep away from fire or flame
    • For external use only

    When using this product

    Do not use in or near eyes. 

    Stop use and ask a doctor

    if irritation or redness develops. If condition persists for more than 72 hours consult a doctor.

    Keep out of reach of children.

    If swallowed, seek immediate medical attention or call a poison control center.

  • Directions

    Wet hands thoroughly with product and allow to dry without wiping.

  • Inactive ingredients

    Water (Aqua), Isopropyl Alcohol, Aloe Barbadensis Leaf Juice, Carbomer, Diisopropylamine, Glycerin, Isopropyl Myristate.

  • PRINCIPAL DISPLAY PANEL

    Pacific Blue Select™
    Gel Hand Sanitizer
    Fragrance and Dye Free
    455mL (15.3 FL OZ)
    Georgia-Pacific Consumer Products LP
    Atlanta, GA 30303-2529
    Made in Mexico
    ©2017 Georgia-Pacific Professional.
    All rights reserved.
    Unless otherwise noted, all trademarks are owned by
    or licensed to Georgia-Pacific Consumer Products LP.

    43341 Label

  • INGREDIENTS AND APPEARANCE
    PACIFIC BLUE SELECT GEL HAND SANITIZER FRAGRANCE AND DYE FREE 
    ethyl alcohol liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:54622-308
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL67 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    ISOPROPYL ALCOHOL (UNII: ND2M416302)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
    POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
    SODIUM SULFITE (UNII: VTK01UQK3G)  
    CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)  
    DIISOPROPYLAMINE (UNII: BR9JLI40NO)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:54622-308-0112 in 1 BOX10/11/2017
    1455 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333E10/11/2017
    Labeler - Georgia-Pacific Consumer Products (806142217)
    Registrant - CYAN Labs S.A. de C.V. (812754130)
    Establishment
    NameAddressID/FEIBusiness Operations
    CYAN Labs S.A. de C.V.812754130manufacture(54622-308) , label(54622-308) , pack(54622-308)