Label: PACIFIC BLUE ULTRA FOAMING FRAGRANCE FREE- ethyl alcohol solution

  • NDC Code(s): 54622-122-01
  • Packager: Georgia-Pacific Consumer Products LP
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 15, 2023

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  • Active ingredient

    Ethyl Alcohol 70% v/v

  • Purpose

    Antiseptic

  • Uses

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

    • FLAMMABLE, keep away from fire and flame
    • For external use only
  • WHEN USING

    When using this product do not use in or near eyes.

  • STOP USE

    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

    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, Isopropyl Alcohol, PEG-12 Dimethicone, Glycerin, Caprylic/Capric Triglyceride, Isopropyl Myristate

  • Additional rear label text

    Pacific Blue Ultra

    Foam Hand Sanitizer

    Fragrance Free SKU 43335

    Manufactured for

    Georgia-Pacific Consumer Products. Atlanta, GA 30303

    Quesitons? Call 1-866-HELLOGP (435-5647)

    or visit us online at www.gppro.com

    (c) 2019 GP PRO. All rights reserved.

    alcohol permit SDS-KY-15002

    43335-B2 PRD Rev A

  • principal display panel

    Foam Hand Sanitizer

    1000 mL (33.8 FL OZ)

    container label

    container labelPBb

    container labelPBAb

  • INGREDIENTS AND APPEARANCE
    PACIFIC BLUE ULTRA FOAMING  FRAGRANCE FREE
    ethyl alcohol solution
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:54622-122
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL70 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    ISOPROPYL ALCOHOL (UNII: ND2M416302)  
    PEG-12 DIMETHICONE (UNII: ZEL54N6W95)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    GLYCERYL CAPRYLATE/CAPRATE (UNII: G7515SW10N)  
    ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:54622-122-011000 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product06/11/2021
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)06/11/2021
    Labeler - Georgia-Pacific Consumer Products LP (806142217)
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