Label: QUALITY CHOICE ANTI-ITCH CLEAR- zinc acetate and pramoxine hydrochloride lotion

  • NDC Code(s): 63868-097-06
  • Packager: Chain Drug Market Association
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 28, 2023

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  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • Active Ingredients

    Zinc Acetate 8%

    Pramoxine HCl 1%

  • Purpose

    Skin Protectant

    External analgesic

  • Uses

    Dries the oozing and weeping, and temporarily relieves pain and itching of poison ivy, oak, and sumac or other skin irritations.

  • Warnings

    For external use only. Use only as directed.

    When using this product. Avoid contact with eyes and moucous membranes.

    Ask a doctor before using on children 2 years of age.

  • Stop use and ask a doctor if

    condition worsens. Symptoms last for more than 7 days or clear up and occur again whitin a few days.

  • Keep out of reach of children.

    In case of accidental ingestion, seek profesional assistance or contact a Poison Control Center immediately.

  • Directions

    Adults and children 2 yr. of age and older. Shake well before using. Cleanse the skin with soap and water and let dry. Apply to the affected area using cotton or soft cloth, not more than 3 to 4 times daily as needed for comfort.

    Children under 2 yrs. of age. Consult a doctor before use.

  • Inactive Ingredients

    SD Alcohol 38B 2.5%, Camphor, Diazolidinyl Urea, Fragrances, Glycerin, Hydroxypropyl Methycelulose, Methylparaben, Polysorbate 80, Propylene Glycol, Propylparaben and Purified Water.

  • Other information

    Store at room temperature 15-30C (59-86F)

  • Principal display panel

    QCCaldyCapture

  • INGREDIENTS AND APPEARANCE
    QUALITY CHOICE ANTI-ITCH CLEAR 
    zinc acetate and pramoxine hydrochloride lotion
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:63868-097
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC CATION - UNII:13S1S8SF37) ZINC CATION80 mg  in 1 mL
    PRAMOXINE HYDROCHLORIDE (UNII: 88AYB867L5) (PRAMOXINE - UNII:068X84E056) PRAMOXINE HYDROCHLORIDE10 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX)  
    METHYLPARABEN (UNII: A2I8C7HI9T)  
    POLYSORBATE 80 (UNII: 6OZP39ZG8H)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    PROPYLPARABEN (UNII: Z8IX2SC1OH)  
    WATER (UNII: 059QF0KO0R)  
    ALCOHOL (UNII: 3K9958V90M)  
    CAMPHOR (NATURAL) (UNII: N20HL7Q941)  
    DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:63868-097-06177 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product12/12/2017
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01603/25/1998
    Labeler - Chain Drug Market Association (011920774)
    Registrant - Pharma Nobis, LLC (118564114)
    Establishment
    NameAddressID/FEIBusiness Operations
    Pharma Nobis, LLC118564114analysis(63868-097) , manufacture(63868-097) , pack(63868-097) , label(63868-097)
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