Label: WALGREEN ANTI-ITCH- pramoxine hcl lotion

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 11, 2023

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  • Active Ingredients

    Pramoxine HCl 1% External analgesic

  • Uses

    temporary relieves pain and itching due to:

    insect bites

    minor burns

    sunburn

    minor skin irritations

    minor cuts

    scrapes

    rashes due to poison ivy, poison oak, and poison sumac

    dries the oozing and weeping of poison:

    ivy

    oak

    sumac

  • Warning

    For external use only

    Do not use

    in the eyes or nose

    over large areas of the body for prolonged periods

    Ask doctor before use

    on chicken pox

    on measles

    When using this product

    do not get into eyes

    Stop Use and ask doctor if

    condition worsens

    symptoms last more than 7 days or clear up and occur again within a few days

    Keep out of reach of children

    If swallowed, get medical help or contact a Poison Control Center right away.

  • Purpose

    Anti - itch

  • Directions

    to open, squeeze cap tightly and turn pump counter-clockwise

    adults and children 2 years and older: apply to affected area not more than 3 to 4 times daily

    children under 2 years: ask a doctor

  • Other information

    store at 20 °C to 25 °C (68 °F to 77 °F)

  • Inactive ingredients

    benzyl alcohol, carbomer 940, cetyl alcohol, dimethicone, glyceryl stearate, isopropyl myristate, PEG-40 stearate,
    PEG-100 stearate, purified water, sodium hydroxide, stearic acid, white petrolatum

  • Principal Display Panel

    Principal Display Panel

    Walgreens

    Compare to Sarna Sensitive Anti-Itch Lotion

    Sensitive Formula Anti-Itch Lotion

    Pramoxine Hydrochloride 1 percent

    Steroid Free

    Reduces and Relieves Itching associated with eczema, dry and sensitive skin

  • INGREDIENTS AND APPEARANCE
    WALGREEN ANTI-ITCH 
    pramoxine hcl lotion
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0363-0263
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    PRAMOXINE HYDROCHLORIDE (UNII: 88AYB867L5) (PRAMOXINE - UNII:068X84E056) PRAMOXINE HYDROCHLORIDE1 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    BENZYL ALCOHOL (UNII: LKG8494WBH)  
    ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)  
    STEARIC ACID (UNII: 4ELV7Z65AP)  
    GLYCERYL STEARATE/PEG-100 STEARATE (UNII: RD25J5V947)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    WATER (UNII: 059QF0KO0R)  
    DIMETHICONE 350 (UNII: 2Y53S6ATLU)  
    PEG-40 STEARATE (UNII: ECU18C66Q7)  
    CARBOMER 940 (UNII: 4Q93RCW27E)  
    PETROLATUM (UNII: 4T6H12BN9U)  
    Product Characteristics
    ColorwhiteScore    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0363-0263-75212 g in 1 BOTTLE, PUMP; Type 0: Not a Combination Product12/08/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01712/08/2020
    Labeler - Walgreens (008965063)
    Registrant - Weeks & Leo, Inc. (005290028)
    Establishment
    NameAddressID/FEIBusiness Operations
    WEEKS & LEO COMPANY, INC.005290028manufacture(0363-0263)
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