EZ ACCESS (BENZOCAINE) LIQUID [PRODUCT MAX GROUP INC]

EZ ACCESS (BENZOCAINE) LIQUID [PRODUCT MAX GROUP INC]
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NDC 70742-001-01
Set ID 94c5bd2d-56d4-46a1-a3bc-e6c2e6c6df86
Category HUMAN OTC DRUG LABEL
Packager Product Max Group Inc
Generic Name
Product Class
Product Number
Application Number PART348
  • Drug FactsActive Ingredient

    Benzocaine 5%

  • Purpose

    Topical Analgesic

  • 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.
  • Uses

    • For temporary relief of pain or soreness in the perianal area.
  • Warnings

    For external use only.

    • Avoid contact with the eyes.
    • Certain persons can develop allergic reactions from ingredients in this product. If the symptom being treated does not subside or if redness, irritation, swelling, pain or other symptoms develop or increase, discontinue use a consult a doctor.

  • Directions

    • When practical, cleanse the affected area with mild soap and water and rinse thoroughly.
    • Gently dry by patting or blotting with a tissue or a soft cloth before the application of this product.
    • Apply to the affected area up to 6 times daily.
  • Other information

    Do not use if safety tab is broken or missing

  • Inactive Ingredients

    Methylparaben, PEG-8, Propylene Glycol, Propylparaben, Water

  • EZ ACCESS product label

    Anal Desensitizer

    EZ ACCESS

    DESENSITIZING SPRAY
    BENZOCAINE ANORECTAL SPRAY

    1.0 FL OZ (30mL)

    www.bodyactionproducts.com

    Distributed by: BodyAction Products, Lutz, FL 33559

    action BODY products

    PMG Ez Access

  • INGREDIENTS AND APPEARANCE
    EZ ACCESS 
    benzocaine liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:70742-001
    Route of AdministrationTopical
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZOCAINE (UNII: U3RSY48JW5) (BENZOCAINE - UNII:U3RSY48JW5) BENZOCAINE1417 mg  in 30 mL
    Inactive Ingredients
    Ingredient NameStrength
    METHYLPARABEN (UNII: A2I8C7HI9T)  
    POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    PROPYLPARABEN (UNII: Z8IX2SC1OH)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:70742-001-0130 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product06/15/2016
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart34806/15/2016
    Labeler - Product Max Group Inc (134893911)
    Registrant - Product Max Group Inc (134893911)

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