TATTOO AFTER CARE A AND D (LANOLIN AND PETROLATUM) OINTMENT [NATUREPLEX LLC]

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TATTOO AFTER CARE A AND D (LANOLIN AND PETROLATUM) OINTMENT [NATUREPLEX LLC]
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NDC 67234-066-01
Set ID e12667d7-31a4-4a15-a7de-8f46191f80e3
Category HUMAN OTC DRUG LABEL
Packager Natureplex LLC
Generic Name
Product Class
Product Number
Application Number PART347
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  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • ACTIVE INGREDIENT

    Active ingredientsPurpose
    Lanolin 15.5%Skin protectant
    Petrolatum 53.4%Skin protectant
  • Uses

    • temporarily protects minor:
      • cuts
      • scrapes
      • burns
    • temporarily protects chapped or cracked skin and lips
  • Warnings

    For external use only.

    When using this product

    • do not get into eyes

    Stop use and ask a doctor if

    • condition worsens
    • symptoms last more than 7 days or clear up and occur again within a few days

    Do not use on

    • deep or puncture wounds
    • animal bites
    • serious burns

    Keep out of reach of children. If swallowed, get medical help, or contact a Poison Control Center right away: 800-222-1222.

  • Direction

    • For skin protectant use: apply as needed
  • Other information

    • store at 15 to 30°C (59 to 86°F)
    • Tamper Evident: DO NOT USE IF SAFETY SEAL ON TUBE IS BROKEN OR MISSING
  • Inactive ingredients

    beeswax, cod liver oil (contains vitamin A & vitamin D), fragrance, microcrystalline wax, mineral oil

  • Questions or Comments?

    866-323-0107 or www.natureplex.com

  • SPL UNCLASSIFIED SECTION

    *This product is manufactured and distributed by Natureplex™.

  • PRINCIPAL DISPLAY PANEL - 42.5 g Tube Carton

    NDC# 67234-066-01

    Natureplex

    TATTOO
    AFTER
    CARE

    A&D OINTMENT
    SKIN PROTECTANT

    NET WT. 1.5 Oz. (42.5g)

    For additional stability, this carton is
    larger than the tube

    Principal Display Panel - 42.5 g Tube Carton
  • INGREDIENTS AND APPEARANCE
    TATTOO AFTER CARE   A AND D
    lanolin and petrolatum ointment
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:67234-066
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    Lanolin (UNII: 7EV65EAW6H) (Lanolin - UNII:7EV65EAW6H) Lanolin0.15 mg  in 1 g
    Petrolatum (UNII: 4T6H12BN9U) (Petrolatum - UNII:4T6H12BN9U) Petrolatum0.53 mg  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    WHITE WAX (UNII: 7G1J5DA97F)  
    COD LIVER OIL (UNII: BBL281NWFG)  
    MINERAL OIL (UNII: T5L8T28FGP)  
    MICROCRYSTALLINE WAX (UNII: XOF597Q3KY)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:67234-066-011 in 1 CARTON06/15/2018
    142.5 g in 1 TUBE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart34706/15/2018
    Labeler - Natureplex LLC (062808196)
    Establishment
    NameAddressID/FEIBusiness Operations
    Natureplex LLC062808196MANUFACTURE(67234-066)
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