Label: COMPUTER EYE RELIEF- conium maculatum and natrium muriaticum and ruta graveolens and senega officinalis solution/ drops
- NDC Code(s): 59262-347-11
- Packager: Similasan Corporation
- 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 October 2, 2020
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Warnings
• For external use only.
• According to homeopathic principles, symptoms may temporarily worsen before improving (Initial exacerbation of symptoms).
• Replace cap tightly after every use.
• To avoid contamination, do not touch the tip of the bottle to any surface.
• To avoid contamination use within 30 days of opening. Expiration date only refers to unopened bottle.
• Contact wearers: consult a physician prior to using.
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INGREDIENTS AND APPEARANCE
COMPUTER EYE RELIEF
conium maculatum and natrium muriaticum and ruta graveolens and senega officinalis solution/ dropsProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:59262-347 Route of Administration OPHTHALMIC Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CONIUM MACULATUM FLOWERING TOP (UNII: Q28R5GF371) (CONIUM MACULATUM FLOWERING TOP - UNII:Q28R5GF371) CONIUM MACULATUM FLOWERING TOP 6 [hp_X] in 10 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) (SODIUM CATION - UNII:LYR4M0NH37) SODIUM CHLORIDE 6 [hp_X] in 10 mL RUTA GRAVEOLENS FLOWERING TOP (UNII: N94C2U587S) (RUTA GRAVEOLENS FLOWERING TOP - UNII:N94C2U587S) RUTA GRAVEOLENS FLOWERING TOP 6 [hp_X] in 10 mL POLYGALA SENEGA ROOT (UNII: M7T6H7D4IF) (POLYGALA SENEGA ROOT - UNII:M7T6H7D4IF) POLYGALA SENEGA ROOT 6 [hp_X] in 10 mL Inactive Ingredients Ingredient Name Strength BORIC ACID (UNII: R57ZHV85D4) SILVER SULFATE (UNII: 8QG6HV4ZPO) SODIUM NITRATE (UNII: 8M4L3H2ZVZ) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:59262-347-11 10 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product 07/02/2013 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 07/02/2013 Labeler - Similasan Corporation (111566530)