AXE CREW CUT BUZZED LOOK WITH SUNSCREEN SPF 15 (OCTINOXATE, OXYBENZONE, OCTISALATE) CREAM [CONOPCO INC. D/B/A UNILEVER]

AXE CREW CUT BUZZED LOOK WITH SUNSCREEN SPF 15 (OCTINOXATE, OXYBENZONE, OCTISALATE) CREAM [CONOPCO INC. D/B/A UNILEVER]
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NDC 64942-1161-1, 64942-1161-2
Set ID f5393bd6-ff10-4bed-affe-57521fbf6cfd
Category HUMAN OTC DRUG LABEL
Packager CONOPCO Inc. d/b/a Unilever
Generic Name
Product Class
Product Number
Application Number PART352
  • ACTIVE INGREDIENT

    Active ingredients
    Octinoxate 7.0%, Oxybenzone 3.0%, Octisalate 1.0%
  • PURPOSE

    Purpose
    Sunscreen
  • INDICATIONS & USAGE

    Uses
    helps prevent sunburn
    higher SPF gives more sunburn protection
    provides moderate protection from sunburn
  • WARNINGS

    Warnings
    For external use only.

    If swallowed, get medical help or contact a Poison Control Center right away.

    When using this product keep out of eyes.  Rinse with water to remove.

    Stop use and ask a doctor if rash or irritation develops.

    Keep out of reach of children.
  • DOSAGE & ADMINISTRATION

    Directions
    Rub onto head and scalp before sun exposure and as needed.  Children under 6 months of age: ask a doctor.
  • INACTIVE INGREDIENT

    Inactive ingredients
    Water, Glycerin, Beeswax, Cetearyl Alcohol, Glyceryl Stearate, VP/VA Copolymer, Sodium Behenoyl Lactylate, Fragrance, Carbomer, Triethanolamine, DMDM Hydantoin, Disodium EDTA, Iodopropynyl Butylcarbamate.
  • QUESTIONS

    Questions?
    Visit us at www.TheAxeEffect.com or call us at 1-800-450-7580 Mon-Fri 8:30am - 6:00pm EST
  • PRINCIPAL DISPLAY PANEL

    Axe Buzzed Cut PDP front
    Axe Buzz SPF15 front  PDP
  • PRINCIPAL DISPLAY PANEL

    Axe Buzz SPF15 back 1
    Axe Buzz SPF15 back 1
  • PRINCIPAL DISPLAY PANEL

    Axe Buzz SPF15 back 2
    Axe Buzz SPF15 back 2
  • PRINCIPAL DISPLAY PANEL

    Axe Buzz SPF15 back 3
    Axe Buzz SPF15 back 3
  • INGREDIENTS AND APPEARANCE
    AXE CREW CUT  BUZZED LOOK WITH SUNSCREEN SPF 15
    octinoxate, oxybenzone, octisalate cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:64942-1161
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE7.0 g  in 100 g
    OXYBENZONE (UNII: 95OOS7VE0Y) (OXYBENZONE - UNII:95OOS7VE0Y) OXYBENZONE3.0 g  in 100 g
    OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE1.0 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    WHITE WAX (UNII: 7G1J5DA97F)  
    CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)  
    GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    DMDM HYDANTOIN (UNII: BYR0546TOW)  
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB)  
    CARBOMER HOMOPOLYMER TYPE C (UNII: 4Q93RCW27E)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:64942-1161-175 g in 1 CONTAINER
    2NDC:64942-1161-215 g in 1 CONTAINER
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart35212/08/2010
    Labeler - CONOPCO Inc. d/b/a Unilever (001375088)
    Establishment
    NameAddressID/FEIBusiness Operations
    Conopco Inc. d/b/a Unilever198786444manufacture

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