Label: APT T3X TETRACYCLINE HYDROCHLORIDE FIRST AID ANTIBIOTIC- tetracycline hydrochloride ointment

  • NDC Code(s): 72053-002-01
  • Packager: Patient Focused Tele-Health, LLC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 1, 2023

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  • Drug Facts

  • Active ingredient (in each gram)

    Tetracycline Hydrochloride 30 mg

    Purpose

    First Aid Antibiotic

  • Use

    First aid to help prevent skin infection in minor cuts, scrapes, and burns.

  • Warnings

    For external use only.

    Do not use

    • longer than 1 week unless directed by a doctor 
    • in the eyes 
    • over large areas of the body

    Ask a doctor before use if you have

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

    Stop use and ask a doctor if

    condition persists or gets worse.

    Keep out of reach of children.

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

  • Directions

    • Clean the affected area. 
    • Apply a small amount of this product (an amount equal to the surface area of the tip of a finger) on the area 1 to 3 times daily) to 3 times daily. 
    • May be covered with a sterile bandage.
  • Inactive ingredients

    Ascorbic Acid, Aloe Barbadensis Leaf Juice, Carbomer, Cholecalciferol, Citric Acid, Diazolidinyl Urea, Dimethyl Sulfoxide, Dipropylene Glycol, DMDM Hydantoin, Glycerin, Polysorbate 20, Sodium Dodecylbenzene Sulfonate, Tetrasodium EDTA, Tocopheryl Acetate, Triethanolamine, Water

  • Package Labeling:

    Box

    02

  • INGREDIENTS AND APPEARANCE
    APT T3X TETRACYCLINE HYDROCHLORIDE FIRST AID ANTIBIOTIC 
    tetracycline hydrochloride ointment
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:72053-002
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    TETRACYCLINE HYDROCHLORIDE (UNII: P6R62377KV) (TETRACYCLINE - UNII:F8VB5M810T) TETRACYCLINE HYDROCHLORIDE30 mg  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    ASCORBIC ACID (UNII: PQ6CK8PD0R)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)  
    CHOLECALCIFEROL (UNII: 1C6V77QF41)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)  
    DIMETHYL SULFOXIDE (UNII: YOW8V9698H)  
    DIPROPYLENE GLYCOL (UNII: E107L85C40)  
    DMDM HYDANTOIN (UNII: BYR0546TOW)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    POLYSORBATE 20 (UNII: 7T1F30V5YH)  
    SODIUM DODECYLBENZENESULFONATE (UNII: 554127163Y)  
    EDETATE SODIUM (UNII: MP1J8420LU)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:72053-002-011 in 1 BOX09/01/2020
    13 g in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00409/01/2020
    Labeler - Patient Focused Tele-Health, LLC (081008911)
    Establishment
    NameAddressID/FEIBusiness Operations
    TG Labs, Inc.831504621manufacture(72053-002)
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