Label: DRYNESS RELIEF- silver, sodium chloride, nutmeg, ruta graveolens, sulfur, zinc liquid

  • 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 September 10, 2021

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

  • Active Ingredients

    Active IngredientsPurpose
    Argentum nitricum HPUS 10XAching, dry feeling eyes
    Natrum muriaticum HPUS 6XInitiates tears, dry eyes
    Nux moschata HPUS 12XLack of tears, dry eyes
    Ruta graveolens HPUS 8XEye strain
    Sulphur HPUS 9XDryness and redness
    Zincum metallicum HPUS 12xExtreme dryness

    “HPUS” indicates the active ingredients are in the Homeopathic Pharmacopoeia of the United States.

  • Purpose

    Argentum nitricum - Aching, dry feeling eyes
    Natrum muriaticum - Initiates tears, dry eyes
    Nux moschata - Lack of tears, dry eyes
    Ruta graveolens - Eye strain
    Sulphur - Dryness and redness
    Zincum metallicum - Extreme dryness

  • Uses*

    Uses:*

    According to homeopathic indications these ingredients provide temporary relief from symptoms such as: • Extreme dryness • Redness • Lack of tears • Eye strain • Achy eyes; after serious causes have been ruled out by a physician. *These statements are based upon traditional homeopathic practice. They have not been reviewed by the Food and Drug Administration.

  • Warnings

    Warnings:

    A PHYSICIAN SHOULD ALWAYS BE CONSULTED TO RULE OUT SERIOUS CAUSES.


    For External Use Only.

    • This product is intended to complement, not replace, standard medical treatment. • Initial worsening of symptoms may occur.

    Contact lens wearers consult physician prior to using.
    To avoid contamination - do not touch tip to any surface.
    Replace cap after every use.
    Use within 30 days of opening.
    EXPIRATION DATE ONLY REFERS TO THE UNOPENED BOTTLE.
    The use of this container by more than one person may spread infection.

  • PREGNANCY OR BREAST FEEDING

    • If pregnant or breast-feeding, ask a health professional before use.
  • Keep out of reach of children

    • Keep out of reach of children. • In case of accidental ingestion, get medical help or contact a Poison Control Center right away.

  • Do not use:

    • If solution changes color or becomes cloudy.
    • If you frequently contract infections that do not clear up easily.
  • Stop use and ask a doctor if:

    • • You experience eye pain or change in vision, continued redness or irritation of the eye.
    • • The condition worsens.
    • • Symptoms last longer than 72 hours.
  • Directions

    Directions:

    • Suitable for adults and children ages 2 and over. Children under the age of 2: Consult a physician before use. • Squeeze 1-3 drops in the eye. Use several times per day as needed. • Homeopathic remedies may not be effective for everyone. Individual results may vary.

  • SPL UNCLASSIFIED SECTION

    Other information:

    • Non-prescription drug products cannot treat infections.

    • Store at room temperature 15° to 30° C (59° to 86°F)

    • Keep bottle tightly closed.

    • Active ingredients are micro-diluted in accordance with the Homeopathic Pharmacopoeia of the United States and are therefore non-toxic with no known side effects or contraindications.

    • Eye Lid Relief® Homeopathic Sterile Eye Drops are homeopathic dilutions, for details see www.thereliefproducts.com

  • INACTIVE INGREDIENT

    Inactive Ingredients:

    Benzalkonium Chloride (preservative), Purified water, Sodium Chloride, Sodium Phosphate DiBasic, Sodium Phosphate Monobasic

  • Questions or comments?

    www.thereliefproducts.com, 1-888-969-6855

  • Principal Display Panel

    Carton

    Label

    FDA Disclaimer: Claims based on traditional homeopathic practice, not medical evidence. Not FDA evaluated.

  • INGREDIENTS AND APPEARANCE
    DRYNESS RELIEF 
    silver, sodium chloride, nutmeg, ruta graveolens, sulfur, zinc liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:17312-178
    Route of AdministrationOPHTHALMIC
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SULFUR (UNII: 70FD1KFU70) (SULFUR - UNII:70FD1KFU70) SULFUR9 [hp_X]  in 1 mL
    RUTA GRAVEOLENS FLOWERING TOP (UNII: N94C2U587S) (RUTA GRAVEOLENS FLOWERING TOP - UNII:N94C2U587S) RUTA GRAVEOLENS FLOWERING TOP8 [hp_X]  in 1 mL
    NUTMEG (UNII: AEE24M3MQ9) (NUTMEG - UNII:AEE24M3MQ9) NUTMEG12 [hp_X]  in 1 mL
    SILVER (UNII: 3M4G523W1G) (SILVER - UNII:3M4G523W1G) SILVER10 [hp_X]  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) (SODIUM CATION - UNII:LYR4M0NH37) SODIUM CHLORIDE6 [hp_X]  in 1 mL
    ZINC (UNII: J41CSQ7QDS) (ZINC - UNII:J41CSQ7QDS) ZINC12 [hp_X]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)  
    WATER (UNII: 059QF0KO0R)  
    SODIUM PHOSPHATE, DIBASIC (UNII: GR686LBA74)  
    SODIUM PHOSPHATE, MONOBASIC (UNII: 3980JIH2SW)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:17312-178-151 in 1 PACKAGE01/11/2021
    110 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved homeopathic01/11/2021
    Labeler - TRP Company (105185719)
    Registrant - TRP Company (105185719)