Label: HAND SANITIZER COASTAL SURF- 62% ethyl alcohol spray

  • 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 25, 2021

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

View All Sections
  • Active ingredient

    Ethyl Alcohol 62%

    Purpose

    Antiseptic

  • Uses

    Helps reduce bacteria on the skin

    recommended for repeated use

  • Warnings

    For external use only

    Flammable, keep away from fire, sparks, and sources of ignition. Do not store above 104 oF/40 oC

    When using this product keep out of eyes. In case of contact with eyes, flush thoroughly with water. Avoid contact with broken skin.

    Stop use and ask a doctor if irritation and redness develop and persist for more than 72 hours.

    Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center immediately.

  • Directions

    Spray directly on hands and rub un thoroughly

    For children under 6, use adult supervision

    Not recommended for infants

  • Inactive Ingredients

    Aloe Barbadensis Leaf Juice, Amyl Cinnamal, Amyris Balsamifera Bark Oil, Anisaldehyde, Benzyl Acetate, Calendula Officinalis Flower Extract, Chamomilla Recutita (Matricaria) Flower Extract, Citral, Citrus Limon (Lemon) Peel Oil, Decanol, Gamma-Decalactone, Gamma-Nonalactone, Geraniol, Glycerin, Hydroxycitronellal, Ionone, Isoamyl Salicylate, Juniperus Virginiana Oil, Limonene, Methyl Anthranilate, Water

  • 2 oz bottle label

    2 oz bottle

  • INGREDIENTS AND APPEARANCE
    HAND SANITIZER  COASTAL SURF
    62% ethyl alcohol spray
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69366-310
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL62 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    CITRAL (UNII: T7EU0O9VPP)  
    GERANIOL (UNII: L837108USY)  
    IONONE (UNII: QP734LIN1K)  
    JUNIPERUS VIRGINIANA OIL (UNII: PAD4FN7P2G)  
    METHYL ANTHRANILATE (UNII: 981I0C1E5W)  
    CHAMOMILE (UNII: FGL3685T2X)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    .ALPHA.-AMYLCINNAMALDEHYDE (UNII: WC51CA3418)  
    BENZYL ACETATE (UNII: 0ECG3V79ZJ)  
    P-ANISALDEHYDE (UNII: 9PA5V6656V)  
    LEMON OIL (UNII: I9GRO824LL)  
    DECANAL (UNII: 31Z90Q7KQJ)  
    WATER (UNII: 059QF0KO0R)  
    CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    AMYRIS BALSAMIFERA OIL (UNII: I1BJ961J2E)  
    .GAMMA.-NONALACTONE (UNII: I1XGH66S8P)  
    ISOAMYL SALICYLATE (UNII: M25E4ZMR0N)  
    LIMONENE, (+)- (UNII: GFD7C86Q1W)  
    .GAMMA.-DECALACTONE (UNII: 7HLS05KP9O)  
    HYDROXYCITRONELLAL (UNII: 8SQ0VA4YUR)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:69366-310-0459 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product07/31/2017
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A07/31/2017
    Labeler - The Honest Company (969962757)
    Registrant - The Honest Company (969962757)
View All Sections

Find additional resources

(also available in the left menu)

Safety

Report Adverse Events, FDA Safety Recalls, Presence in Breast Milk

Related Resources

Medline Plus, Clinical Trials, PubMed, Biochemical Data Summary

More Info on this Drug

View Labeling Archives, RxNorm, Get Label RSS Feed, View NDC Code(s)NEW!