Label: COMPUTER EYE RELIEF- conium maculatum, natrium muriaticum, ruta graveolens, senega officinalis solution/ drops
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Contains inactivated NDC Code(s)
NDC Code(s): 59262-355-01, 59262-355-13 - 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 March 20, 2019
If you are a consumer or patient please visit this version.
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- Official Label (Printer Friendly)
- Active Ingredient
- Purpose
- Active Ingredient
- Purpose
- Active Ingredient
- Purpose
- Active Ingredient
- Purpose
- Uses
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Warnings
- For external use only.
- Initial exacerbation of symptoms may occur.
- Use only if single-use dropper is intact.
- To avoid contamination, do not touch the tip of the dropper to any surface. Do not reuse. Once opened, discard.
- Contact wearers: consult a physician prior to using.
- Directions
- Inactive Ingredients
- Principal Display Panel
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INGREDIENTS AND APPEARANCE
COMPUTER EYE RELIEF
conium maculatum, natrium muriaticum, ruta graveolens, senega officinalis solution/ dropsProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:59262-355 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 0.45 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) (SODIUM CATION - UNII:LYR4M0NH37) SODIUM CHLORIDE 6 [hp_X] in 0.45 mL RUTA GRAVEOLENS FLOWERING TOP (UNII: N94C2U587S) (RUTA GRAVEOLENS FLOWERING TOP - UNII:N94C2U587S) RUTA GRAVEOLENS FLOWERING TOP 6 [hp_X] in 0.45 mL POLYGALA SENEGA ROOT (UNII: M7T6H7D4IF) (POLYGALA SENEGA ROOT - UNII:M7T6H7D4IF) POLYGALA SENEGA ROOT 6 [hp_X] in 0.45 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) SODIUM PHOSPHATE, MONOBASIC, DIHYDRATE (UNII: 5QWK665956) SODIUM PHOSPHATE, DIBASIC, ANHYDROUS (UNII: 22ADO53M6F) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:59262-355-01 200 in 1 CARTON 07/01/2011 1 .45 mL in 1 VIAL, SINGLE-USE; Type 0: Not a Combination Product 2 NDC:59262-355-13 .45 mL in 1 VIAL, SINGLE-USE; Type 0: Not a Combination Product 07/01/2011 12/31/2018 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date UNAPPROVED HOMEOPATHIC 07/01/2011 Labeler - Similasan Corporation (111566530)