Label: DAISY DND- alcohol spray

  • Category: HUMAN OTC DRUG LABEL

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 June 10, 2020

If you are a healthcare professional or from the pharmaceutical industry please visit this version.

View All Sections
  • Active Ingredient

    Ethyl Alcohol 75% v/v.

  • Purpose

    Antiseptic

  • Use[s]

    • to decrease bacteria on the skin that could cause disease
    • recommended for repeated use
  • Warnings

    For external use only- hands.
    Flammable, keep away from heat or flame.
    Do not use

    • in children less than 2 months of age
    • on open skin wounds

    When using this product

    • keep out of eyes, in case of contact with eyes, rinse eyes thoroughly with water.
    • avoid contact with broken skin.
    • do not inhale or ingest.

    Stop use and ask a doctor if skin irritation develops.

  • KEEP OUT OF REACH OF CHILDREN

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

  • Directions

    • Spray on to hands and allow to dry without wiping.
    • For children under 6, use only under adult supervision.
    • Not recommended for infants.
  • Other information

    • Store between 20°C-25°C (68-77°F).
    • May discolor certain fabrics and surfaces.
  • Inactive ingredients

    Water (Aqua), Jojoba oil

  • Package Label - Principal Display Panel

    Label 80 mL

    Label 100 mL

  • INGREDIENTS AND APPEARANCE
    DAISY DND 
    alcohol spray
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:78951-004
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL75 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    JOJOBA OIL (UNII: 724GKU717M)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:78951-004-0180 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product04/26/2020
    2NDC:78951-004-02240 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product04/26/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A04/26/2020
    Labeler - Daisy Nail Product Inc. (038797014)
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

More Info on this Drug

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