Label: ALCOHOL spray
ALCOHOL 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 February 9, 2021

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

View All Sections
  • ACTIVE INGREDIENT

    Ethyl Alcohol - 62.0%

  • PURPOSE

    Antiseptic

  • USES:

    For hand washing to decrease bacteria on skin

    • Recommended for repeated use.
  • WARNINGS:

    For external use only

    • Flammable
    • Keep away from fire/flame

    • Do not use this product in or near eyes. If contact occurs rinse thoroughly with water

    • Keep out of reach of children
    • If swallowed, get medical help or contact a Poison Control Center right away
    • Children under six years of age should be supervised.
  • DIRECTIONS:

    Dispense an adequate amount in your palm to cover all surfaces of hands completely

    • Rub hands together until dry
    • Does not require rinsing.
  • OTHER INFORMATION:

    Do not store above 104°F/40°C.

    • May discolor some fabrics.
  • INACTIVE INGREDIENTS:

    Aloe Barbadensis Leaf Juice. Chamomile Extract Carbomer, Glycerin, Natural Vitamin E (tocopheryl acetate), Panthenol, Propylene Glycol, Purified Water, Triethanolamine

  • Principal Display Panel – 118 mL Bottle Label

    Non-sterile Solution

    hello
    bello™

    Alcohol Antiseptic 80%
    Topical Solution

    80% Alcohol

    Hand Sanitizer
    Spray

    4 fl. oz. (118 ml) e

    Principal Display Panel – 118 mL Bottle Label
  • Principal Display Panel – 354 mL Bottle Label

    hello
    bello™

    Fragrance-Free

    Kills Germs

    Hand Sanitizer
    Gel

    12 fl. oz. (354 ml) e

    Principal Display Panel – 354 mL Bottle Label
  • Principal Display Panel – 59 mL Bottle Label

    hello
    bello™

    Fragrance-Free

    Made with Aloe
    and Chamomile Extracts.

    Kills Germs

    Hand Sanitizer
    Gel

    2.0 fl. oz. (59 ml) e

    Principal Display Panel – 59 mL Bottle Label
  • INGREDIENTS AND APPEARANCE
    ALCOHOL 
    alcohol spray
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:73418-039
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    Alcohol (UNII: 3K9958V90M) (Alcohol - UNII:3K9958V90M) Alcohol80 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    Glycerin (UNII: PDC6A3C0OX)  
    Hydrogen Peroxide (UNII: BBX060AN9V)  
    Water (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:73418-039-01118 mL in 1 BOTTLE; Type 0: Not a Combination Product04/01/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A04/01/2020
    ALCOHOL 
    alcohol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:73418-040
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    Alcohol (UNII: 3K9958V90M) (Alcohol - UNII:3K9958V90M) Alcohol70 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    Water (UNII: 059QF0KO0R)  
    Aloe Vera Leaf (UNII: ZY81Z83H0X)  
    Glycerin (UNII: PDC6A3C0OX)  
    CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:73418-040-01354 mL in 1 BOTTLE; Type 0: Not a Combination Product04/01/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A04/01/2020
    ALCOHOL 
    alcohol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:73418-041
    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
    Aloe Vera Leaf (UNII: ZY81Z83H0X)  
    Chamomile (UNII: FGL3685T2X)  
    CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)  
    Glycerin (UNII: PDC6A3C0OX)  
    .Alpha.-Tocopherol Acetate (UNII: 9E8X80D2L0)  
    Panthenol (UNII: WV9CM0O67Z)  
    Propylene Glycol (UNII: 6DC9Q167V3)  
    Water (UNII: 059QF0KO0R)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:73418-041-0159 mL in 1 BOTTLE; Type 0: Not a Combination Product04/01/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A04/01/2020
    Labeler - Hello Bello (081135707)
    Establishment
    NameAddressID/FEIBusiness Operations
    Unconditional Love081135707MANUFACTURE(73418-039, 73418-040, 73418-041)
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!