Label: TETRA NOW 3%- tetracycline hcl 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 December 2, 2021

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  • ACTIVE INGREDIENT

    TETRACYCLINE HCL 30 MG

  • PURPOSE

    TOPICAL ANTIBIOTIC OINTMENT

  • USE(S)

    • FIRST AID TO HELP PREVENT SKIN INFECTION IN MINOR CUTS, SCRAPES, AND BURNS
  • WARNINGS

    FOR EXTERNAL USE ONLY.

    DO NOT USE

    • IF YOU HAVE AN ALLERGY TO ANY INGREDIENT
    • IN THE EYES
    • OVER LARGE AREAS OF THE BODY

    CONSULT A DOCTOR BEFORE USE IF YOU HAVE

    • DEEP OR PUNCTURE WOUNDS
    • SERIOUS BURNS
    • ANIMAL BITES
    • DIABETES AND A WOUND ON THE FOOT
    • YOU NEED TO USE LONGER THAN 1 WEEK
    • CONDITIONS PERSIST OR GET WORSE
    • RASH OR ALLERGIC REACTION DEVELOPS

    IF PREGNANT OR BREAST-FEEDING CONSULT A DOCTOR BEFORE USE.

  • KEEP OUT OF REACH OF CHILDREN

    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 TWICE DAILY. MAY BE COVERED WITH A STERILE BANDAGE.
  • INACTIVE INGREDIENTS

    BHT, PARAFINNUM LIQUIDUM, POLYETHYLENE

  • QUESTIONS?

    1-845-422-4571

    WWW.TETRANOW.CO

    ADVANCED CLINICAL MANAGEMENT, 1175 W. BITTERS RD. STE. 2102, SAN ANTONIO, TX 78216

  • PRINCIPAL DISPLAY PANEL

    01b UC_TetraNow_BoxFinal_210928

  • INGREDIENTS AND APPEARANCE
    TETRA NOW  3%
    tetracycline hcl ointment
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:81871-101
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    TETRACYCLINE HYDROCHLORIDE (UNII: P6R62377KV) (TETRACYCLINE - UNII:F8VB5M810T) TETRACYCLINE HYDROCHLORIDE3 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)  
    HIGH DENSITY POLYETHYLENE (UNII: UG00KM4WR7)  
    MINERAL OIL (UNII: T5L8T28FGP)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:81871-101-111 in 1 BOX12/02/2021
    17.5 g in 1 TUBE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart333B12/02/2021
    Labeler - ADVANCED CLINICAL MANAGEMENT LLC (118026938)
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