Label: SUAVE- essentials ocean breeze hand sanitizer gel

  • 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 August 31, 2022

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  • SUAVE ESSENTIALS OCEAN BREEZE HAND SANITIZER - Ethyl Alcohol gel

    Suave Skin Solutions Hand Sanitizer Lotion

  • Drug Facts

    Active ingredient

    Ethyl Alcohol 75.60%

  • Purpose

    Antiseptic

  • Uses

    helps decrease bacteria on the hands

  • Warnings

    For external use only
    Flammable. Keep away from fire or flame
    Do not store in car.
    Avoid contact with eyes,     In case of contact, rinse eyes thoroughly with water.
    If irritation develops, discontinue use and consult a doctor.

  • KEEP OUT OF REACH OF CHILDREN

    • Keep out of reach of children except under adult supervision.

    If swallowed, get medical help or contact a poison control Center right away.

  • Directions

    Wet hand thoroughly with product and rub lightly until dry. Do not wipe off or rinse

  • Other information

    • May discolor fabrics or surfaces.
    • Store below 105˚F (40˚C).

  • Inactive ingredients

    Water (Aqua), Glycerin, Fragrance (Parfum), Hydroxypropylcellulose, Lauryl Lactate, Myristyl Lactate, Cetyl Lactate, Cocos Nucifera (Coconut) Oil, Aloe Barbadensis Leaf Juice, Blue 1 (CI 42090) Red 33 (CI 17200).

  • Call

    1-800-782-8301 or visit www.suave.com

  • Packaging

    Suave Ocean Breeze Sanitizer

  • INGREDIENTS AND APPEARANCE
    SUAVE 
    essentials ocean breeze hand sanitizer gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:64942-2043
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL75.6 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    HYDROXYPROPYL CELLULOSE, UNSPECIFIED (UNII: 9XZ8H6N6OH)  
    LAURYL LACTATE (UNII: G5SU0BFK7O)  
    MYRISTYL LACTATE (UNII: 1D822OC34X)  
    WATER (UNII: 059QF0KO0R)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    COCONUT OIL (UNII: Q9L0O73W7L)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    D&C RED NO. 33 (UNII: 9DBA0SBB0L)  
    CETYL LACTATE (UNII: A7EVH2RK4O)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:64942-2043-1236 mL in 1 BOTTLE; Type 0: Not a Combination Product06/02/2022
    2NDC:64942-2043-259 mL in 1 BOTTLE; Type 0: Not a Combination Product06/02/2022
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A06/02/2022
    Labeler - Conopco Inc. d/b/a/ Unilever (001375088)
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