Label: VASELINE- clinical care hand sanitizer lotion lotion

  • NDC Code(s): 64942-1849-1, 64942-1849-2, 64942-1849-4
  • Packager: Conopco Inc. d/b/a/ Unilever
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph not 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 May 16, 2022

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  • VASELINE CLINICAL CARE HAND SANITIZER LOTION - Benzalkonium Chloride lotion

    Vaseline Clinical Care Hand Sanitizer Lotion

  • Drug Facts

    Active ingredient

    Benzalkonium Chloride 0.13%

  • Purpose

    Antibacterial

  • Uses

    helps decrease bacteria on the hands

  • Warnings

    For external use only
    Avoid contact with eyes,     In case of contact, rinse eyes thoroughly with water.
    If irritation develops, discontinue use and consult a doctor .

    .

  • KEEP OUT OF REACH OF CHILDREN

    • Keep out of reach of children except under adult supervision.

    If swallowed, get medical help or contact a poison control Center right away.

  • Directions

    Apply product thoroughly to hands. Rub hands together until absorbed. Do not wipe off or rinse. Apply to hands as needed.

  • Inactive ingredients

    Water (Aqua), Glycerin, Tapioca Starch, Polyquaternium-37, Dicaprylyl Carbonate, Phenoxyethanol, Caprylyl Glycol, Fragrance (Parfum), Lauryl Glucoside, Tocopheryl Acetate, Citronellol, Limonene, Linalool, Titanium Dioxide (CI 77891)

  • Questions or Comments?

    1-800-457-7964

  • PRINCIPAL DISPLAY PANEL

    Vaseline Hand Sanitizer LotionPackaging

  • INGREDIENTS AND APPEARANCE
    VASELINE 
    clinical care hand sanitizer lotion lotion
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:64942-1849
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE1.3 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    STARCH, TAPIOCA (UNII: 24SC3U704I)  
    POLYQUATERNIUM-37 (10000 MPA.S) (UNII: 41QWS48DFN)  
    DICAPRYLYL CARBONATE (UNII: 609A3V1SUA)  
    WATER (UNII: 059QF0KO0R)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
    LAURYL GLUCOSIDE (UNII: 76LN7P7UCU)  
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    .BETA.-CITRONELLOL, (R)- (UNII: P01OUT964K)  
    LIMONENE, (+)- (UNII: GFD7C86Q1W)  
    LINALOOL, (+/-)- (UNII: D81QY6I88E)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:64942-1849-188.5 mL in 1 TUBE; Type 0: Not a Combination Product01/29/2021
    2NDC:64942-1849-2150 mL in 1 TUBE; Type 0: Not a Combination Product01/29/2021
    3NDC:64942-1849-4236 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product01/29/2021
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333E01/29/2021
    Labeler - Conopco Inc. d/b/a/ Unilever (001375088)
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