Label: CHAMOMILE HOMEOPATHIC EYE DROPS solution/ drops

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

DISCLAIMER: This homeopathic product has not been evaluated by the Food and Drug Administration for safety or efficacy. FDA is not aware of scientific evidence to support homeopathy as effective.

Drug Label Information

Updated December 12, 2018

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  • Inactive ingredients

    Purified water
    Sodium chloride
    Sodium phosphate di-basic
    Potassium phosphate
    Benzalkonium chloride

  • Purpose

    Dryness

    Inflammation

  • DOSAGE & ADMINISTRATION

    Uses To refresh and replenish moisture to eyes.
    Directions 2 drops in each eye as needed.
    To avoid contamination, do not touch tip of dropper to any surface.
    Replace cap immediately after use.
    Store at room temperature.
    Use within 30 days of opening.

  • Warnings

    For ophtalmic use only. Keep out of the reach of chlidren. Do not use is solution changes color or becomes cloudy. Discard 30 days after opening. Stop use and ask a doctor if you experience eye pain, changes in vision, redness or irritation of the eye. If conditions persist or worsen for more than 72 hours, discontinue use and consult your physician.


    Do not use is cap safety band is torn or missing.

    Active Ingredients

    Chamomilla 3X HPUS

  • INDICATIONS & USAGE

    Uses To refresh and replenish moisture to eyes.
    Directions 2 drops in each eye as needed.
    To avoid contamination, do not touch tip of dropper to any surface.
    Replace cap immediately after use.
    Store at room temperature.
    Use within 30 days of opening.

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of the reach of children.

  • Label

    SterileEyeDropsSri.jpg

    Chamomile Homeopathic Eye Drops

    SterileEyeDropsSri.jpg

  • INGREDIENTS AND APPEARANCE
    CHAMOMILE HOMEOPATHIC EYE DROPS 
    chamomile homeopathic eye drops solution/ drops
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:61727-346(NDC:70696-346)
    Route of AdministrationOPHTHALMIC
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    MATRICARIA CHAMOMILLA WHOLE (UNII: 2Z4LRR776S) (MATRICARIA CHAMOMILLA WHOLE - UNII:2Z4LRR776S) MATRICARIA CHAMOMILLA WHOLE3 [hp_X]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM PHOSPHATE, DIBASIC (UNII: GR686LBA74)  
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)  
    POTASSIUM PHOSPHATE, UNSPECIFIED FORM (UNII: B7862WZ632)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:61727-346-1515 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product05/23/2016
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved homeopathic05/23/2016
    Labeler - HomeoCare Laboratories Inc. (088248828)
    Registrant - HomeoCare Laboratories Inc. (088248828)
    Establishment
    NameAddressID/FEIBusiness Operations
    HomeoCare Laboratories Inc.088248828relabel(61727-346)
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