Label: COMPUTER EYE RELIEF- conium maculatum and natrium muriaticum and ruta graveolens and senega officinalis 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 October 2, 2020

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

  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • Active Ingredients

    Conium maculatum 6X

  • Purpose

    light sensitivity, aching

  • Active Ingredients

    Natrum muriaticum 6X

  • Purpose

    burning, redness, eye strain

  • Active Ingredients

    Ruta graveolens 6X

  • Purpose

    eye strain, pressure

  • Active Ingredients

    Senega officinalis 6X

  • Purpose

    aching, dryness, eye strain, light sensitivity

  • Uses*

    According to homeopathic principles, the active ingredients in this product temporarily relieve minor symptoms such as:

    • tired, aching eyes

    • burning

    • redness

    • strained eyes (Computer, TV, reading, driving)

  • Warnings

    • For external use only.

    • According to homeopathic principles, symptoms may temporarily worsen before improving (Initial exacerbation of symptoms).

    • Replace cap tightly after every use.

    • To avoid contamination, do not touch the tip of the bottle to any surface.

    • To avoid contamination use within 30 days of opening. Expiration date only refers to unopened bottle.

    • Contact wearers: consult a physician prior to using.

    If pregnant, trying to get pregnant or breast feeding,

    ask a health professional before use.

    Keep out of reach of children.

    If swallowed, get medical help or contact a Poison Control Center right away.

    Do not use:

    • if the solution changes color or becomes cloudy.

    Stop use and ask a doctor if:

    • symptoms worsen or persist for more than 72 hours

    • you experience eye pain or changes in vision

  • Directions

    For adults and children age 2 and over:

    • remove tamper-evident seal from neck of bottle

    • twist cap off bottle

    DON'T squeeze bottle, squeeze plastic tip to release 2 to 3 drops into eye

    • apply as needed

    • replace cap after use

  • Other Information

    Active ingredients are manufactured according to homeopathic principles.

  • Inactive Ingredients

    Borate buffer, Purified water, Silver sulfate (as preservative), Sodium nitrate

  • Questions?

    Reach our representatives at 1-800-240-9780 or getinfo@similasanusa.com.

    www.SimilasanUSA.com

  • PRINCIPAL DISPLAY PANEL

    NDC 59262-347-11

    Computer
    Eye Relief
    STERILE
    EYE DROPS
    10 ml/ 0.33 fl oz

    PRINCIPAL DISPLAY PANEL
NDC 59262-347-11
Computer
Eye Relief
STERILE
EYE DROPS
10 ml/ 0.33 fl oz

  • INGREDIENTS AND APPEARANCE
    COMPUTER EYE RELIEF 
    conium maculatum and natrium muriaticum and ruta graveolens and senega officinalis solution/ drops
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:59262-347
    Route of AdministrationOPHTHALMIC
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CONIUM MACULATUM FLOWERING TOP (UNII: Q28R5GF371) (CONIUM MACULATUM FLOWERING TOP - UNII:Q28R5GF371) CONIUM MACULATUM FLOWERING TOP6 [hp_X]  in 10 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) (SODIUM CATION - UNII:LYR4M0NH37) SODIUM CHLORIDE6 [hp_X]  in 10 mL
    RUTA GRAVEOLENS FLOWERING TOP (UNII: N94C2U587S) (RUTA GRAVEOLENS FLOWERING TOP - UNII:N94C2U587S) RUTA GRAVEOLENS FLOWERING TOP6 [hp_X]  in 10 mL
    POLYGALA SENEGA ROOT (UNII: M7T6H7D4IF) (POLYGALA SENEGA ROOT - UNII:M7T6H7D4IF) POLYGALA SENEGA ROOT6 [hp_X]  in 10 mL
    Inactive Ingredients
    Ingredient NameStrength
    BORIC ACID (UNII: R57ZHV85D4)  
    SILVER SULFATE (UNII: 8QG6HV4ZPO)  
    SODIUM NITRATE (UNII: 8M4L3H2ZVZ)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:59262-347-1110 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product07/02/2013
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved homeopathic07/02/2013
    Labeler - Similasan Corporation (111566530)