Label: ORAL SORE ANTISEPTIC- hydrogen peroxide, menthol liquid

  • 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 September 2, 2022

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

  • active ingredients

    Hydrogen peroxide 1.5% (w/v)

    Menthol 0.1% (w/v)

  • purpose

    Oral debriding agent/Oral antiseptic
    Oral pain reliever

  • uses

    ▪ first aid to help protect against bacterial contamination in minor oral wounds
    ▪ for temporary pain relief and ▪ temporary use in cleansing minor wounds or minor gum inflammation resulting from: ▪ minor dental procedures ▪  dentures ▪ orthodontic appliances ▪ accidental injury ▪ other irritations of the mouth and gums ▪ canker sores
    ▪ aids in the removal of: ▪ phlegm ▪ mucus ▪ other secretions associated with occasional sore mouthUses
    ▪ first aid to help protect against bacterial contamination in minor oral wounds
    ▪ for temporary pain relief and ▪ temporary use in cleansing minor wounds or minor gum inflammation resulting from: ▪ minor dental procedures ▪  dentures
    ▪ orthodontic appliances ▪ accidental injury ▪ other irritations of the mouth and gums ▪ canker sores
    ▪ aids in the removal of: ▪ phlegm ▪ mucus ▪ other secretions associated with occasional sore mouth

  • warnings

    Stop use and ask a doctor if
    ▪ sore throat is severe, persists for more than 2 days, is accompanied or followed by fever, headache, rash, nausea, or vomiting
    ▪ irritation, pain, or redness persists or worsens
    ▪ swelling, rash, or fever develops
    ▪ sore mouth symptoms do not improve in 7 days

  • When using this product

    •  do not swallow 
    •  do not use more than 7 days unless directed by a dentist or doctor 
    •  do not exceed recommended dosage
  • Keep out of reach of children

    If more than used for rinsing is accidentally swallowed, get medical help or contact a Poison Control Center right away

  • directions

    Adults and children 2 years of age and older - swish two teaspoons (10 mL) around the mouth for at least 1 minute, then spit out; use up to 4 times daily or as directed by a dentist or physician

    Children under 12 years of age - should be supervised in the use of the product

    Children under 2 years of age - consult a dentist or doctor

  • other information

    • store at controlled room temperature 68-77°F (20-25°C) 
    • keep away from heat or direct sunlight
  • inactive ingredients

    alcohol (4.1% v/v), blue 1, disodium EDTA, methyl salicylate, phosphoric acid, poloxamer 338, polysorbate 20, sodium saccharin, sorbitol, water

  • SAFETY SEAL

    SEALED WITH PRINTED NECKBAND FOR YOUR PROTECTION

  • questions

    Call 1-800-925-4733

  • ADVERSE REACTIONS SECTION

    DISTRIBUTED BY: WALGREEN CO., 200 WILMOT RD., DEERFIELD, IL 60015

    100% SATISFACTION GUARANTEED  walgreens.com 

    MADE IN U.S.A. WITH U.S. AND FOREIGN COMPONENTS

    Our pharmacist recommend the Walgreens brand.  We invite you to compare to national brands.

    This product is not manufacted or distributed by

    Church & Dwight Co., Inc owner of the trademark Orajel

  • Principal display panel

    Walgreens

    WALGREENS - PHARMACIST RECOMMENDED

    Compare to the active ingredients in Orael Antiseptic Rinse

    Antiseptic

    Rinse

    ORAL PAIN RELIEVER & DEBRIDING AGEN WITH HYDROGEN PEROXIDE & MENTHOL

    Cleans Mouth Sores

    • For mouth sores, including gum irritation from braces or dentures & canker sores
    • Temporary pain relief for mouth sores
    • Kills germs & bacterial

    Mint flavor

    16 FL OZ (473 mL)

    SEALED WITH PRINTED NECKBAND FOR YOUR PROTECTION

    image description

  • INGREDIENTS AND APPEARANCE
    ORAL SORE ANTISEPTIC 
    hydrogen peroxide, menthol liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0363-1045
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    HYDROGEN PEROXIDE (UNII: BBX060AN9V) (HYDROGEN PEROXIDE - UNII:BBX060AN9V) HYDROGEN PEROXIDE1.5 mg  in 1 mL
    MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL1 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    ALCOHOL (UNII: 3K9958V90M)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)  
    METHYL SALICYLATE (UNII: LAV5U5022Y)  
    PHOSPHORIC ACID (UNII: E4GA8884NN)  
    POLOXAMER 338 (UNII: F75JV2T505)  
    POLYSORBATE 20 (UNII: 7T1F30V5YH)  
    SACCHARIN SODIUM (UNII: SB8ZUX40TY)  
    SORBITOL (UNII: 506T60A25R)  
    water (UNII: 059QF0KO0R)  
    Product Characteristics
    Color    Score    
    ShapeSize
    FlavorMINTImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0363-1045-43473 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product03/15/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart35603/15/2020
    Labeler - Walgreens (008965063)
    Registrant - Vi-Jon, LLC (790752542)
    Establishment
    NameAddressID/FEIBusiness Operations
    VI-Jon, LLC790752542manufacture(0363-1045)
    Establishment
    NameAddressID/FEIBusiness Operations
    VI-Jon, LLC088520668manufacture(0363-1045)