Label: MOONSTAR HAIR 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 March 1, 2018

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  • Active ingredient

    Potassium carbonate (0.1%)

  • Purpose

    antibacterial

  • Uses

    Sanitizer to help decrease bacteria on scalp. Helps to clean and hydrate hair and scalp. To stimulate hair growth and thicken hair.

  • Warnings

    For external use only

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

    When using this product

    • do not use on damaged or broken scalp
    • 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 scalp 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

    Mist hair and scalp daily to cleanse, hydrate, and nourish.

  • Inactive ingredients

    Distilled Water, ε-Polylysine, Hydroxypropylmethyl Cellulose, Citric Acid, Tea Catechin, Calcium hydroxide

  • MOONSTAR HAIR MIST

    hair  mist

  • INGREDIENTS AND APPEARANCE
    MOONSTAR HAIR MIST 
    potassium carbonate spray
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:72111-101
    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)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    WATER (UNII: 059QF0KO0R)  
    CALCIUM HYDROXIDE (UNII: PF5DZW74VN)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:72111-101-0180 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 other03/01/2018
    Labeler - NATURAL ETHICS, INC. (081069540)
    Registrant - NATURAL ETHICS, INC. (081069540)
    Establishment
    NameAddressID/FEIBusiness Operations
    NATURAL ETHICS, INC.081069540relabel(72111-101)
    Establishment
    NameAddressID/FEIBusiness Operations
    NARO, INC694590211manufacture(72111-101)