Label: VACATION INSTANT BROWNING- avobenzone octisalate octocrylene lotion

  • NDC Code(s): 80641-521-10, 80641-521-80
  • Packager: Vacation Inc.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated March 6, 2024

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

  • Dosage and administration

    Apply liberally 15 minutes before sun exposure.

    Reapply at least every 2 hours.

    Use water-resistent sunscreen if swimming or sweating

  • Warnings

    For external use only

    Do not use on damaged or broken skin

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

    Stop use and ask a doctor if rash occurs

    In case of ingestion, get medical help or contact a Poison Control Center right away

  • Inactives

    OCTISALATE, OCTOCRYLENE, ACETYL L-TYROSINE, LEVOMENOL, MAGNESIUM STEARATE, OCTYLDODECYL OLEATE, WATER, C13-15 ALKANE, PROPANEDIOL, COCOA BUTTER, TOCOPHEROL, VANILLA PLANIFOLIA OIL, DOCOSANOL, DECYL GLUCOSIDE, SODIUM METABISULFITE, PORPHYRIDIUM PURPUREUM, ALCOHOL, BUTYLOCTYL SALICYLATE, BUTYROSPERMUM PARKII (SHEA) BUTTER UNSAPONIFIABLES, CAPRYLHYDROXAMIC ACID, CAPRYLYL GLYCOL, CETOSTEARYL ALCOHOL, CETYL ALCOHOL, CITRIC ACID MONOHYDRATE, COCO GLUCOSIDE, ARABICA COFFEE OIL, EUROPEAN HAZELNUT OIL, DIHYDROXYACETONE, DIMETHICONE, ETHYLENE BRASSYLATE, ETHYL FERULATE, GLYCERIN, FERRIC OXIDE RED, LAURYL GLUCOSIDE, PASSIFLORA EDULIS SEED OIL, CHASTE TREE

  • Indications and Usage

    Helps prevent sunburn

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

  • Keep out of reach of children

    Keep out of reach of childen

    In case of ingestion, get medical help or contact a Poison Control Center right away

  • Purpose

    Sunscreen

  • Vacation Browning Lotion

    Browning Lotion 5oz

  • INGREDIENTS AND APPEARANCE
    VACATION INSTANT BROWNING 
    avobenzone octisalate octocrylene lotion
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:80641-521
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE2.9 g  in 100 mL
    OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE9.5 g  in 100 mL
    OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE4.9 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    ACETYL L-TYROSINE (UNII: DA8G610ZO5)  
    LEVOMENOL (UNII: 24WE03BX2T)  
    MAGNESIUM STEARATE (UNII: 70097M6I30)  
    OCTYLDODECYL OLEATE (UNII: MCA43PK7MH)  
    WATER (UNII: 059QF0KO0R)  
    C13-15 ALKANE (UNII: 114P5I43UJ)  
    PROPANEDIOL (UNII: 5965N8W85T)  
    COCOA BUTTER (UNII: 512OYT1CRR)  
    TOCOPHEROL (UNII: R0ZB2556P8)  
    VANILLA PLANIFOLIA OIL (UNII: 0A3F415158)  
    DOCOSANOL (UNII: 9G1OE216XY)  
    DECYL GLUCOSIDE (UNII: Z17H97EA6Y)  
    SODIUM METABISULFITE (UNII: 4VON5FNS3C)  
    PORPHYRIDIUM PURPUREUM (UNII: K2P8K2558N)  
    ALCOHOL (UNII: 3K9958V90M)  
    BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)  
    BUTYROSPERMUM PARKII (SHEA) BUTTER UNSAPONIFIABLES (UNII: 0C9AC7D6XU)  
    CAPRYLHYDROXAMIC ACID (UNII: UPY805K99W)  
    CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
    CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)  
    CETYL ALCOHOL (UNII: 936JST6JCN)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    COCO GLUCOSIDE (UNII: ICS790225B)  
    ARABICA COFFEE OIL (UNII: IK55HKE887)  
    EUROPEAN HAZELNUT OIL (UNII: 8RQ2839AVG)  
    DIHYDROXYACETONE (UNII: O10DDW6JOO)  
    DIMETHICONE (UNII: 92RU3N3Y1O)  
    ETHYLENE BRASSYLATE (UNII: 9A87HC7ROD)  
    ETHYL FERULATE (UNII: 5B8915UELW)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    FERRIC OXIDE RED (UNII: 1K09F3G675)  
    LAURYL GLUCOSIDE (UNII: 76LN7P7UCU)  
    PASSIFLORA EDULIS SEED OIL (UNII: F3VOA31UHQ)  
    CHASTE TREE (UNII: 433OSF3U8A)  
    SODIUM GLUCONATE (UNII: R6Q3791S76)  
    APRICOT SEED OIL (UNII: 54JB35T06A)  
    SODIUM STEAROYL GLUTAMATE (UNII: 65A9F4P024)  
    TRIHEPTANOIN (UNII: 2P6O7CFW5K)  
    XANTHAN GUM (UNII: TTV12P4NEE)  
    METHYL DIHYDROABIETATE (UNII: 7666FJ0J9F)  
    ARACHIDYL ALCOHOL (UNII: 1QR1QRA9BU)  
    CARROT SEED OIL (UNII: 595AO13F11)  
    ERYTHRULOSE, D- (UNII: 09058VOU0Z)  
    HYALURONIC ACID (UNII: S270N0TRQY)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:80641-521-10148 mL in 1 BOTTLE; Type 0: Not a Combination Product03/06/2024
    2NDC:80641-521-8030 mL in 1 BOTTLE; Type 0: Not a Combination Product03/06/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM02003/06/2024
    Labeler - Vacation Inc. (117644631)