Label: WOUND CARE- wound care ointment ointment

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph 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 November 10, 2021

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  • Active Ingredients

    Zinc Oxide--0.5%

  • Inactive Ingredients

    Bees Wax, Linoleic Acid, Propolis, Sesame Oil and a combination of all-natural Chinese Herbs

  • Keep out of reach of children.

    If swallowed, call poison control or seek medical help.

  • Consulting a doctor before using

    on deep or puncture wounds, animal bites or serious burns.

  • Stop use and ask a doctor

    if your condition worsens, does not improve, persists for more than 7 days, or occurs again after a few days.

  • Purpose

    Skin Protectant

  • Other information

    Store at room temperature. may stain fabrics

  • Directions

    Wash with mild skin cleanser. Pat dry or allow to air dry. Apply an ample amount of ointment over affected skin. Cover with a clean bandage. Repeat procedure every 12 hours until skin improves or as directed by a doctor.

  • Dosage & administration

  • When using this product

    Do not get into eyes

  • Warnings

    For external use only,

    When using this product do not get into eyes

  • Label

    01020304

  • INGREDIENTS AND APPEARANCE
    WOUND CARE 
    wound care ointment ointment
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:73252-133
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE0.5 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    LINOLEIC ACID (UNII: 9KJL21T0QJ)  
    PROPOLIS WAX (UNII: 6Y8XYV2NOF)  
    SESAME OIL (UNII: QX10HYY4QV)  
    YELLOW WAX (UNII: 2ZA36H0S2V)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:73252-133-0225 g in 1 BOTTLE; Type 0: Not a Combination Product05/07/2019
    2NDC:73252-133-0350 g in 1 BOTTLE; Type 0: Not a Combination Product05/07/2019
    3NDC:73252-133-04100 g in 1 BOTTLE; Type 0: Not a Combination Product05/07/2019
    4NDC:73252-133-0115 g in 1 BOTTLE; Type 0: Not a Combination Product05/07/2019
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart34705/07/2019
    Labeler - Hunan Xiong Shi Pharmaceutical Co., Ltd (554497403)
    Registrant - Hunan Xiong Shi Pharmaceutical Co., Ltd (554497403)
    Establishment
    NameAddressID/FEIBusiness Operations
    Hunan Xiong Shi Pharmaceutical Co., Ltd.554497403manufacture(73252-133)
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