DRYNESS RELIEF PF- silver, sodium chloride, nutmeg, ruta graveolens, sulfur, zinc liquid 
TRP Company

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.

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Natural Eyes Dryness Relief TM PF

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.

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:

Stop use and ask a doctor if:

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.

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.

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

Inactive Ingredients:

Purified water, Sodium Chloride, Sodium Phosphate DiBasic, Sodium Phosphate Monobasic

Questions or comments?

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

Principal Display Panel

CartonLabel

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

Carton

Label

DRYNESS RELIEF PF 
silver, sodium chloride, nutmeg, ruta graveolens, sulfur, zinc liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:17312-096
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
WATER (UNII: 059QF0KO0R)  
SODIUM PHOSPHATE, DIBASIC (UNII: GR686LBA74)  
SODIUM PHOSPHATE, MONOBASIC (UNII: 3980JIH2SW)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:17312-096-191 in 1 PACKAGE08/09/2022
110 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
2NDC:17312-096-991 in 1 PACKAGE02/22/2023
22.5 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved homeopathic08/09/2022
Labeler - TRP Company (105185719)
Registrant - TRP Company (105185719)

Revised: 2/2023
Document Id: f551534c-7a78-efea-e053-2995a90a8ee8
Set id: e5d491e0-b5e0-704c-e053-2995a90af9dd
Version: 4
Effective Time: 20230222
 
TRP Company