Label: CVS ITCH RELIEF MOISTURIZING- pramoxine hcl 1% lotion

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

Drug Label Information

Updated October 18, 2023

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  • ACTIVE INGREDIENT

    Pramoxine Hydrochloride 1%

  • PURPOSE

    External analgesic

  • INDICATIONS & USAGE

    Use for the temporary relief of itching associated with minor skin irritations

  • WARNINGS

    For external use only

    do not get into eyes

    Stop use and ask a doctor if

    condition worsens

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

    Do not use on

    • animal bites
    • severe puncture wounds or burns
  • KEEP OUT OF REACH OF CHILDREN

    If swallowed, get medical help or contact a Poison Control Immediately (1-800-222-1222)

  • DOSAGE & ADMINISTRATION

    Adults and Children 2 years of age and older: apply to affected area not more than 3 to 4 times daily

    Children under 2 years of age: Consult a doctor

  • INACTIVE INGREDIENT

    Allantion, Aloe Vera, Arginine PCA, Behenic Acid, Ceramide AP, Ceramide EOP, Ceramide NP, Cetearyl Alcohol, Cetyl Alcohol, Cholesterol, Dimethicone, Disodium EDTA, Glycerin, Glyceryl Stearate, Isopropyl Palmitate, Niacinamide, PEG 100 Stearate, Isopropyl Palmitate, Niacinamide, PEG 100 Stearate, Phenoxyethanol, Phytosphingosine, Polyglyceryl-2- Diisostearate, polyglyceryl-6 Behenate, Polyglyceryl-10 Stearate, Potassium Sorbate, Purified water, Shea Butter, Sodium Cetearyl Sulfate, Sodium Levulinate, Sodium PCA, Stearic Acid, Tocopheryl Acetate, Triethanolamine, Triethyl Citrate, Xanthan Gum, Zinc Citrate.

  • PRINCIPAL DISPLAY PANEL

    Package Label frontPackage Label back

  • INGREDIENTS AND APPEARANCE
    CVS ITCH RELIEF MOISTURIZING 
    pramoxine hcl 1% lotion
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:51316-144
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    PRAMOXINE HYDROCHLORIDE (UNII: 88AYB867L5) (PRAMOXINE - UNII:068X84E056) PRAMOXINE HYDROCHLORIDE1 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    CERAMIDE AP (UNII: F1X8L2B00J)  
    ISOPROPYL PALMITATE (UNII: 8CRQ2TH63M)  
    CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)  
    POLYGLYCERYL-3 DISTEARATE (UNII: ZI1LK470XV)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2)  
    ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    XANTHAN GUM (UNII: TTV12P4NEE)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    CERAMIDE NP (UNII: 4370DF050B)  
    WATER (UNII: 059QF0KO0R)  
    SHEA BUTTER (UNII: K49155WL9Y)  
    PEG-100 STEARATE (UNII: YD01N1999R)  
    GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  
    STEARIC ACID (UNII: 4ELV7Z65AP)  
    NIACINAMIDE (UNII: 25X51I8RD4)  
    ZINC CITRATE (UNII: K72I3DEX9B)  
    DIMETHICONE (UNII: 92RU3N3Y1O)  
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    CETYL ALCOHOL (UNII: 936JST6JCN)  
    ALLANTOIN (UNII: 344S277G0Z)  
    ARGININE (UNII: 94ZLA3W45F)  
    CERAMIDE 1 (UNII: 5THT33P7X7)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:51316-144-01237 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product10/17/2023
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01710/17/2023
    Labeler - CVS Health (062312574)
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