Label: DOUBLE-DUTY FACE MOISTURIZER- mositurizing sunscreen lotion

  • NDC Code(s): 66738-020-01, 66738-020-03, 66738-020-04, 66738-020-16, view more
    66738-020-19
  • Packager: Jack Black, LLC
  • 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 January 22, 2020

If you are a consumer or patient please visit this version.

  • Active Ingredients

    Avobenzone   2.2%   Sunscreen

    Octinoxate     7.5%   Sunscreen

  • Use

    Helps prevent sunburn

  • Warnings

    • For external use only
    • Do not use on damaged or broken skin
    • Stop use and ask doctor if rash occurs
    • When using this product keep out of eyes.  Rinse with water to remove
    • Keep out of reach of children
    • If swallowed, get medical help or contact Poison Control Center right away
  • Directions

    • Apply liberally 15 minutes before sun exposure
    • Use a water resisitant sunscreen if swimming or sweating
    • Reapply at least every two hours
    • Children under 6 months: ask a doctor.
    • Sun Protection Measures:
    •    Spending time in the sun increases your risk of skin cancer and early skin aging.  To decrease this risk, use sunscreen with a broad spectrum SPF15 or higher
    •    Limit time in the sun, especxially from 10 a.m. - 2 p.m.
    •    Wear long sleeve shirts, pants, hats and sunglasses.
  • Other Information

    Protect product from excessive heat and driect sunlight.  You may report a serious adverse reaction from using this product to Jack Black at 1-877-766-3388.

  • Questions?

    1-877-766-3388

    www.getjackblack.com

  • Label

    Jack Black Double-Duty Face Moisturizer.jpg

  • INGREDIENTS AND APPEARANCE
    DOUBLE-DUTY FACE MOISTURIZER 
    mositurizing sunscreen lotion
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:66738-020
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE2.2 g  in 1000 g
    OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE7.5 g  in 1000 g
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    CYCLOMETHICONE (UNII: NMQ347994Z)  
    OCTYLDODECYL NEOPENTANOATE (UNII: X8725R883T)  
    PHENETHYL BENZOATE (UNII: 0C143929GK)  
    HASLEA OSTREARIA (UNII: Y87200QHN9)  
    HYALURONATE SODIUM (UNII: YSE9PPT4TH)  
    LECITHIN, SOYBEAN (UNII: 1DI56QDM62)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    LAVENDER OIL (UNII: ZBP1YXW0H8)  
    ROSEMARY OIL (UNII: 8LGU7VM393)  
    MELISSA OFFICINALIS LEAF OIL (UNII: PTP6R7263M)  
    PEUCEDANUM OSTRUTHIUM LEAF (UNII: 86P27YRR6Y)  
    BUDDLEJA DAVIDII LEAF (UNII: X380815D32)  
    PELARGONIUM GRAVEOLENS FLOWER OIL (UNII: 3K0J1S7QGC)  
    DIMETHICONE (UNII: 92RU3N3Y1O)  
    GLYCERETH-26 (UNII: NNE56F2N14)  
    HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER (100000 MPA.S AT 1.5%) (UNII: 86FQE96TZ4)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    CETEARYL GLUCOSIDE (UNII: 09FUA47KNA)  
    CARBOMER 934 (UNII: Z135WT9208)  
    BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB)  
    DULSE (UNII: 7832HOY4ZQ)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)  
    CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD)  
    LEONTOPODIUM NIVALE SUBSP. ALPINUM FLOWER (UNII: MWN6IZU3XM)  
    APPLE FRUIT OIL (UNII: 9NT987I3A8)  
    ARTEMISIA UMBELLIFORMIS FLOWER (UNII: 91OLL9AJ7D)  
    CHAMAEMELUM NOBILE FLOWER OIL (UNII: UB27587839)  
    CARBOMER HOMOPOLYMER TYPE A (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: F68VH75CJC)  
    Product Characteristics
    Colorwhite (Opaque Lotion) Score    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:66738-020-0397 g in 1 BOTTLE; Type 0: Not a Combination Product05/29/2009
    2NDC:66738-020-0444 g in 1 TUBE; Type 0: Not a Combination Product07/30/2009
    3NDC:66738-020-19251 g in 1 BOTTLE; Type 0: Not a Combination Product06/15/2011
    4NDC:66738-020-0130 g in 1 TUBE; Type 0: Not a Combination Product04/01/2020
    5NDC:66738-020-16480 g in 1 BOTTLE; Type 0: Not a Combination Product05/01/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart35205/29/2009
    Labeler - Jack Black, LLC (847024036)