Label: IMAGE PREVENTION PLUS PROFESSIONAL ULTIMATE PROTECTION MOISTURIZER SPF50- homosalate, octisalate, octocrylene, zinc oxide sunscreen cream

  • NDC Code(s): 60232-1026-6
  • Packager: Swiss-American CDMO, LLC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated November 6, 2023

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

  • Warnings

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

  • Keep out of Reach of Children

    Keep out of Reach of Children

  • Active Ingredients

    Homosalate   10%   Sunscreen

    Octisalate   5%   Sunscreen

    Octocrylene   6%   Sunscreen

    Zinc Oxide   9%   Sunscreen

  • Uses

    Helps prevent sunburn. If used as directed with other sun protection measures (see Directions), decreases the risk of skin cancer and early skin aging caused by the sun.

  • Uses

    Helps prevent sunburn. If used as directed with other sun protection measures (see Directions), decreases the risk of skin cancer and early skin aging caused by the sun.

  • Directions For Sunscreen Use

    Apply generously 15 minutes before sun exposure. Children under 6 months of age: ask a doctor. Reapply at least every 2 hours. Use a water resistant sunscreen if swimming or sweating. Immediately after towel drying. At least every 2 hours. Sun Protection Measures. Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease this risk, regularly use a sunscreen with a Broad Spectrum SPF value of 15 or higher and other sun protection measures including: limit time in the sun, especially from 10am to 2pm, wear long-sleeved shirts, pants, hats and sunglasses.

  • Other Information

    Protect the product in this container from excessive heat and direct sun.

  • Inactive Ingredients

    water, caprylic/capric triglyceride, glycerin, cyclopentasiloxane, cetyl PEG/PPG-10/1 dimethicone, thermus thermophillus ferment, polyacrylate-13, cetearyl ethylhexanoate, phenoxyethanol, polyisobutene, polyglyceryl-6 polyricinoleate, lecithin, isostearic acid, polyglyceryl-3 polyricinoleate, polyhydroxystearic acid, soidum chloride, cetearyl dimethicone, marrubium vulgare extract, helianthus annus (sunflower) see oil, disteardimonium hectorite, polysorbate 20, citrus aurantum dulcis (orange) peel oil, limonene, sorbitan isostearate, ethylhexylglycerin, panthenol, citrus nobils (mandarin orange) peel oil, disodium EDTA, sodium hyaluronate, melanin, erythritol, citric acid, vanilla planifolia fruit extract, glucose, potassium sorbate, hydrolyzed pea protein, tocopherol, PEG-8/SMDI copolymer, tetrahexyldecyl ascorbate, tocopheryl acetate, barosma betuuna (buchu) leaf oil, soidum benzoate, homarine HCL, pentaerythrityl tetra-di-t-butylhydroxyhydrocinnamate, sodium succinate, malus domestica fruit cell culture extract, arabidopsis thaliana (thale cress) extract, micrococcus lysate, plankton extract, ergothioneine

  • Questions

    Questions: call 800-796-7546

  • Labeling

    Professional Ultimate Protection

  • INGREDIENTS AND APPEARANCE
    IMAGE PREVENTION PLUS PROFESSIONAL ULTIMATE PROTECTION MOISTURIZER SPF50 
    homosalate, octisalate, octocrylene, zinc oxide sunscreen cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:60232-1026
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE110 g  in 1000 g
    OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE50 g  in 1000 g
    OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE60 g  in 1000 g
    ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC CATION - UNII:13S1S8SF37) ZINC CATION90 g  in 1000 g
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)  
    CETYL PEG/PPG-10/1 DIMETHICONE (HLB 1.5) (UNII: V2W71V8T0X)  
    THERMUS THERMOPHILUS (UNII: 415H64SACF)  
    CETEARYL ETHYLHEXANOATE (UNII: 9M64UO4C25)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    POLYISOBUTYLENE (1000 MW) (UNII: 5XB3A63Y52)  
    LECITHIN, SOYBEAN (UNII: 1DI56QDM62)  
    ISOSTEARIC ACID (UNII: X33R8U0062)  
    POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    CETYL DIMETHICONE 150 (UNII: 5L694Y0T22)  
    MARRUBIUM VULGARE (UNII: 7A72MUN24Z)  
    SUNFLOWER OIL (UNII: 3W1JG795YI)  
    DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)  
    POLYSORBATE 20 (UNII: 7T1F30V5YH)  
    ORANGE OIL (UNII: AKN3KSD11B)  
    LIMONENE, (+/-)- (UNII: 9MC3I34447)  
    SORBITAN ISOSTEARATE (UNII: 01S2G2C1E4)  
    ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
    PANTHENOL (UNII: WV9CM0O67Z)  
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    HYALURONIC ACID (UNII: S270N0TRQY)  
    ERYTHRITOL (UNII: RA96B954X6)  
    ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
    VANILLA BEAN (UNII: Q74T35078H)  
    ANHYDROUS DEXTROSE (UNII: 5SL0G7R0OK)  
    POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
    TOCOPHEROL (UNII: R0ZB2556P8)  
    PEG-8/SMDI COPOLYMER (UNII: CCX72L6NY6)  
    TETRAHEXYLDECYL ASCORBATE (UNII: 9LBV3F07AZ)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    AGATHOSMA BETULINA LEAF OIL (UNII: KOS935A04V)  
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    HOMARINE HYDROCHLORIDE (UNII: 8866LNG61N)  
    PENTAERYTHRITOL TETRAKIS(3-(3,5-DI-TERT-BUTYL-4-HYDROXYPHENYL)PROPIONATE) (UNII: 255PIF62MS)  
    SODIUM SUCCINATE ANHYDROUS (UNII: V8ZGC8ISR3)  
    MALUS DOMESTICA WHOLE (UNII: 04W636S1V3)  
    MICROCOCCUS LUTEUS (UNII: LV6L29Z6AX)  
    ERGOTHIONEINE (UNII: BDZ3DQM98W)  
    Product Characteristics
    ColorwhiteScore    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:60232-1026-6170 g in 1 TUBE; Type 0: Not a Combination Product01/31/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM02001/31/2020
    Labeler - Swiss-American CDMO, LLC (080170933)
    Registrant - Swiss-American CDMO, LLC (080170933)
    Establishment
    NameAddressID/FEIBusiness Operations
    Swiss-American CDMO, LLC080170933manufacture(60232-1026)