Label: MOONSTAR FACE AND BODY MIST- potassium carbonate spray

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved drug other

DISCLAIMER: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

Drug Label Information

Updated February 22, 2018

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  • Active ingredients

    Potassium carbonate (0.1%)

  • Purpsoe

    antibacterial

  • Uses

    Sanitizer to help decrease bacteria on skin. Helps to soothe skin.

  • Warnings

    For external use only

    Do not use when skin is red, inflamed, irritated, or painful

    When using this product

    • do not use on damaged or broken skin
    • avoid contact with eyes. If contact occurs, rinse eyes thoroughly with water
    • do not apply directly to wound or open cut

    Stop use and ask a doctor if

    • Rash or irritation on skin develops and lasts
  • Keep out of reach of children

    If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) right away.

  • DIrections

    Spray daily on face and body to cleanse and refreshes skin. Safe for use on sensitive areas of the body.

  • Inactive ingredients

    Distilled water, Hydroxypropylmethyl Cellulose, Citric Acid, Tea Catechin, Calcium hydroxide

  • MOONSTAR FACE & BODY MIST

    face body mist

  • INGREDIENTS AND APPEARANCE
    MOONSTAR FACE AND BODY MIST 
    potassium carbonate spray
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:72111-100
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    POTASSIUM CARBONATE (UNII: BQN1B9B9HA) (CARBONATE ION - UNII:7UJQ5OPE7D) POTASSIUM CARBONATE0.08 g  in 80 mL
    Inactive Ingredients
    Ingredient NameStrength
    HYPROMELLOSES (UNII: 3NXW29V3WO)  
    WATER (UNII: 059QF0KO0R)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    CALCIUM HYDROXIDE (UNII: PF5DZW74VN)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:72111-100-0180 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product03/01/2018
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other02/27/2018
    Labeler - NATURAL ETHICS, INC. (081069540)
    Registrant - NATURAL ETHICS, INC. (081069540)
    Establishment
    NameAddressID/FEIBusiness Operations
    NATURAL ETHICS, INC.081069540relabel(72111-100)
    Establishment
    NameAddressID/FEIBusiness Operations
    NARO, INC694590211manufacture(72111-100)