NDC | 17312-058-15 |
Set ID | 74af00f8-e844-6ce3-e053-2991aa0ad576 |
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 provide temporary relief from symptoms such as: • Burning • Stinging • Itching • Watering • Redness • Dryness; 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
RedEye Relief Homeopathic Sterile Eye Drops are homeopathic dilutions: see www.trpcompany.com for details.
- INACTIVE INGREDIENT
- Questions or comments?
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
REDEYE RELIEF
apis mellifera, euphrasia stricta, calcium sulfide, loeselia mexicana whole, pulsatilla vulgaris liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:17312-058 Route of Administration OPHTHALMIC Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CALCIUM SULFIDE (UNII: 1MBW07J51Q) (CALCIUM SULFIDE - UNII:1MBW07J51Q) CALCIUM SULFIDE 12 [hp_X] in 1 mL EUPHRASIA STRICTA (UNII: C9642I91WL) (EUPHRASIA STRICTA - UNII:C9642I91WL) EUPHRASIA STRICTA 6 [hp_X] in 1 mL PULSATILLA VULGARIS (UNII: I76KB35JEV) (PULSATILLA VULGARIS - UNII:I76KB35JEV) PULSATILLA VULGARIS 6 [hp_X] in 1 mL LOESELIA MEXICANA WHOLE (UNII: XA8YCV5M3E) (LOESELIA MEXICANA WHOLE - UNII:XA8YCV5M3E) LOESELIA MEXICANA WHOLE 6 [hp_X] in 1 mL APIS MELLIFERA (UNII: 7S82P3R43Z) (APIS MELLIFERA - UNII:7S82P3R43Z) APIS MELLIFERA 6 [hp_X] in 1 mL Inactive Ingredients Ingredient Name Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) WATER (UNII: 059QF0KO0R) SODIUM CHLORIDE (UNII: 451W47IQ8X) SODIUM PHOSPHATE, DIBASIC (UNII: GR686LBA74) SODIUM PHOSPHATE, MONOBASIC (UNII: 3980JIH2SW) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:17312-058-15 1 in 1 PACKAGE 06/01/2018 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 06/01/2018 Labeler - TRP Company (105185719) Registrant - TRP Company (105185719)