Label: REDEYE RELIEF- apis mellifera, euphrasia stricta, calcium sulfide, loeselia mexicana whole, pulsatilla vulgaris liquid
- NDC Code(s): 17312-058-15, 17312-058-99
- 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.
Drug Label Information
Updated February 9, 2023
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- Official Label (Printer Friendly)
- Active Ingredients
- PURPOSE
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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
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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
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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 2 NDC:17312-058-99 1 in 1 PACKAGE 02/09/2023 2 2.5 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)