NDC | 17312-172-15 |
Set ID | 74ae6725-48bc-81a2-e053-2a91aa0a4ab7 |
Category | HUMAN OTC DRUG LABEL |
Packager | TRP Company |
Generic Name | |
Product Class | |
Product Number | |
Application Number |
- Active Ingredients
- PURPOSE
-
INDICATIONS & USAGE
Uses:*
According to homeopathic indications these ingredients temporarily relieve minor symptoms such as:
• Eye strain with headache • Double vision • Difficulty focusing • Difficulty reading • Eye fatigue • Sore irritated 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
- PREGNANCY OR BREAST FEEDING
-
WARNINGS
• 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.
- Do not use:
- Stop use and ask a doctor if:
- Keep out of reach of children
- SPL UNCLASSIFIED SECTION
- DOSAGE & ADMINISTRATION
-
SPL UNCLASSIFIED SECTION
Other information:
Non-prescription drug products cannot treat infections.- 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.
- Store at room temperature 15° to 30° C (59° to 86° F).
- Keep bottle tightly closed
• Eye Strain ReliefTM Homeopathic Sterile Eye Drops are homeopathic dilutions, for details see www.thereliefproducts.com. - INACTIVE INGREDIENT
- Questions or comments?
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
EYE STRAIN RELIEF
aconitum napellus - apis mellifera - silver nitrate - euphrasia stricta - sodium arsenate, dibasic, heptahydrate - liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:17312-172 Route of Administration OPHTHALMIC Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength RUTA GRAVEOLENS FLOWERING TOP (UNII: N94C2U587S) (RUTA GRAVEOLENS FLOWERING TOP - UNII:N94C2U587S) RUTA GRAVEOLENS FLOWERING TOP 6 [hp_X] in 1 mL EUPHRASIA STRICTA (UNII: C9642I91WL) (EUPHRASIA STRICTA - UNII:C9642I91WL) EUPHRASIA STRICTA 6 [hp_X] in 1 mL PHYSOSTIGMA VENENOSUM SEED (UNII: CJV9E9IIOA) (PHYSOSTIGMA VENENOSUM SEED - UNII:CJV9E9IIOA) PHYSOSTIGMA VENENOSUM SEED 13 [hp_X] in 1 mL CONIUM MACULATUM FLOWERING TOP (UNII: Q28R5GF371) (CONIUM MACULATUM FLOWERING TOP - UNII:Q28R5GF371) CONIUM MACULATUM FLOWERING TOP 6 [hp_X] in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) (SODIUM CATION - UNII:LYR4M0NH37) SODIUM CHLORIDE 8 [hp_X] in 1 mL POLYGALA SENEGA ROOT (UNII: M7T6H7D4IF) (POLYGALA SENEGA ROOT - UNII:M7T6H7D4IF) POLYGALA SENEGA ROOT 6 [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:17312-172-15 1 in 1 PACKAGE 08/27/2018 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 08/27/2018 Labeler - TRP Company (105185719) Registrant - TRP Company (105185719)