Label: DERMADIVE ULTRACARE - TETRAID- benzalkonium chloride lotion

  • NDC Code(s): 78663-102-34
  • Packager: Releaf Technologies LLC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated November 3, 2023

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  • ACTIVE INGREDIENT

    BENZALKONIUM CHLORIDE 0.13%

  • PURPOSE

    ANTIMICROBIAL

  • USES

    TO PROTECT SKIN AND SPEED HEALING OF WOUNDS AND SORES.

  • WARNING

    FOR EXTERNAL USE ONLY.

    DO NOT USE ON DEEP PUNCTURE WOUNDS OR LACERATIONS.

    WHEN USING THIS PRODUCT AVOID CONTACT WITH THE EYES.

    STOP USING AND ASK A DOCTOR IF

    • THE CONDITION WORSENS
    • A RASH OR IRRITATION DEVELOPS.
  • 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

    APPLY AS NEEDED TO AFFECTED AREAS.

  • OTHER INFORMATION

    PROTECT PRODUCT FROM EXCESSIVE MOISTURE - AVOID STORING IN DIRECT SUNLIGHT - STORE WITH LID TIGHTLY CLOSED.

  • INACTIVE INGREDIENTS

    PURIFIED WATER, GLYCERYL STEARATE, EMULSIFYING WAX, STEARYL ALCOHOL, CETYL ALCOHOL, CYCLOTETRASILOXANE (AND) CYCLOPENTASILOXANE, PHENOXYETHANOL, ETHYLHEXYLGLYCERIN, ETHOXYDIGLYCOL, PROPYLENE GLYCOL, WATER, LECITHIN, ALCOHOL, GLYCERIN, TEA TREE OIL, TRIETHANOLAMINE

  • PRINCIPAL DISPLAY PANEL

    01b LBL_Tetraid_100mL

  • INGREDIENTS AND APPEARANCE
    DERMADIVE ULTRACARE - TETRAID 
    benzalkonium chloride lotion
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:78663-102
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE0.13 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX)  
    GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  
    WATER (UNII: 059QF0KO0R)  
    ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
    DIETHYLENE GLYCOL MONOETHYL ETHER (UNII: A1A1I8X02B)  
    POLYSORBATE 60 (UNII: CAL22UVI4M)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    LECITHIN, SOYBEAN (UNII: 1DI56QDM62)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    STEARYL ALCOHOL (UNII: 2KR89I4H1Y)  
    CYCLOMETHICONE 4 (UNII: CZ227117JE)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    CETYL ALCOHOL (UNII: 936JST6JCN)  
    TEA TREE OIL (UNII: VIF565UC2G)  
    ALCOHOL (UNII: 3K9958V90M)  
    CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:78663-102-34100 mL in 1 TUBE; Type 0: Not a Combination Product08/07/2023
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00308/07/2023
    Labeler - Releaf Technologies LLC (117532647)
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