ITCH RELIEF CLEAR SKIN PROTECTANT CVS (PRAMOXINE HCL, ZINC ACETATE) SPRAY [CVS]

ITCH RELIEF CLEAR SKIN PROTECTANT CVS (PRAMOXINE HCL, ZINC ACETATE) SPRAY [CVS]
PDF | XML

NDC 59779-295-03
Set ID a90049e4-27a5-447c-8d3d-c319c3c7baf7
Category HUMAN OTC DRUG LABEL
Packager CVS
Generic Name
Product Class
Product Number
Application Number PART347
  • Active ingredient

    Pramoxine  HCl 1%

    Zinc Acetate 0.1%

  • Purpose

    Itch Relief.

  • Uses

    • Temporarily relieves pain and itching asociated with:
    • rashes due to poison ivy, poison oak or poison sumac.
    • insect bites.
    • minor skin irritation.
    • minor cuts.
    • dries the oozing and weeping of poison ivy, poison oak and poison sumac.
  • Warnings

    For external use only.

    Flammable: Do not use near heat, flame, or while smoking.

    ​​​

    When using this product

    • keep out of eyes. Rinse with water to remove.
    • Do not puncture or incinerate. Contents under pressure. Do no store at temperatures above 120F.

    Stop use and ask a doctor if

    • condition worsens or does not improve within 7 days.
    • symptoms persist for more than 7 days or clear up and occur again with in a few days.

    Keep out of reach of children

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

  • Directions

    • shake well before use.
    • 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: ask a doctor. 
  • Inactive ingredients

    SD Alcohol 38-B, Avena Sative (Oat Meal) Extract, Camphor, Citric Acid, Diazolidinyl Urea, Fragrance, Glycerin, Hypromellose, Methylparaben,Polysorbate 40, Propylene Glycol, Propylparaben, Sodium Citrate, Water.

  • PRINCIPAL DISPLAY PANEL

    CVS Continuous Spray Itch Relief

    Clear Skin Protectant

    1% Pramoxine HCl

    0.1% Zinc Acetate

    image description

  • INGREDIENTS AND APPEARANCE
    ITCH RELIEF CLEAR SKIN PROTECTANT  CVS
    pramoxine hcl, zinc acetate spray
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:59779-295
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    PRAMOXINE HYDROCHLORIDE (UNII: 88AYB867L5) (PRAMOXINE - UNII:068X84E056) PRAMOXINE HYDROCHLORIDE1 g  in 100 g
    ZINC ACETATE (UNII: FM5526K07A) (ZINC CATION - UNII:13S1S8SF37) ZINC ACETATE.1 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    ALCOHOL (UNII: 3K9958V90M)  
    OATMEAL (UNII: 8PI54V663Y)  
    CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)  
    METHYLPARABEN (UNII: A2I8C7HI9T)  
    POLYSORBATE 40 (UNII: STI11B5A2X)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    PROPYLPARABEN (UNII: Z8IX2SC1OH)  
    SODIUM CITRATE (UNII: 1Q73Q2JULR)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:59779-295-0385 g in 1 CAN; Type 0: Not a Combination Product10/31/2014
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart34710/31/2014
    Labeler - CVS (062312574)
    Registrant - Product Quest Mfg, LLC (927768135)
    Establishment
    NameAddressID/FEIBusiness Operations
    Product Quest Mfg, LLC927768135manufacture(59779-295)

Related Drugs