Label: DRYNESS RELIEF- silver, sodium chloride, nutmeg, ruta graveolens, sulfur, zinc liquid
- NDC Code(s): 17312-178-15
- Packager: TRP Company
- 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.
Updated September 10, 2021
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Active Ingredients Purpose Argentum nitricum HPUS 10X Aching, dry feeling eyes Natrum muriaticum HPUS 6X Initiates tears, dry eyes Nux moschata HPUS 12X Lack of tears, dry eyes Ruta graveolens HPUS 8X Eye strain Sulphur HPUS 9X Dryness and redness Zincum metallicum HPUS 12x Extreme dryness
“HPUS” indicates the active ingredients are in the Homeopathic Pharmacopoeia of the United States.
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.
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
- Keep out of reach of children
- Do not use:
- Stop use and ask a doctor if:
SPL UNCLASSIFIED SECTION
• 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
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INGREDIENTS AND APPEARANCE
silver, sodium chloride, nutmeg, ruta graveolens, sulfur, zinc liquid
Product Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:17312-178 Route of Administration OPHTHALMIC Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SULFUR (UNII: 70FD1KFU70) (SULFUR - UNII:70FD1KFU70) SULFUR 9 [hp_X] in 1 mL RUTA GRAVEOLENS FLOWERING TOP (UNII: N94C2U587S) (RUTA GRAVEOLENS FLOWERING TOP - UNII:N94C2U587S) RUTA GRAVEOLENS FLOWERING TOP 8 [hp_X] in 1 mL NUTMEG (UNII: AEE24M3MQ9) (NUTMEG - UNII:AEE24M3MQ9) NUTMEG 12 [hp_X] in 1 mL SILVER (UNII: 3M4G523W1G) (SILVER - UNII:3M4G523W1G) SILVER 10 [hp_X] in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) (SODIUM CATION - UNII:LYR4M0NH37) SODIUM CHLORIDE 6 [hp_X] in 1 mL ZINC (UNII: J41CSQ7QDS) (ZINC - UNII:J41CSQ7QDS) ZINC 12 [hp_X] in 1 mL Inactive Ingredients Ingredient Name Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) WATER (UNII: 059QF0KO0R) SODIUM PHOSPHATE, DIBASIC (UNII: GR686LBA74) SODIUM PHOSPHATE, MONOBASIC (UNII: 3980JIH2SW) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:17312-178-15 1 in 1 PACKAGE 01/11/2021 1 10 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 01/11/2021 Labeler - TRP Company (105185719) Registrant - TRP Company (105185719)