Label: EYE SUPPORT (allium cepa, symphytum officinale, argentum nitricum, eye- suis, vaccinium myrtillus, apis mellifica, calcarea fluorica, carboneum sulphuratum, cedron, gelsemium sempervirens, kali iodatum, nux moschata, phosphorus, physostigma venenosum, staphysagria liquid
- NDC Code(s): 43742-2083-1
- Packager: Deseret Biologicals, Inc.
- 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 19, 2024
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ACTIVE INGREDIENTS:
Allium Cepa 6X, Apis Mellifica 12X, Argentum Nitricum 6X, 12X, 30X, Calcarea Fluorica 12X, Carboneum Sulphuratum 12X, Cedron 12X, Eye (Suis) 6X, 12X, 30X, Gelsemium Sempervirens 12X, Kali Iodatum 12X, Nux Moschata 12X, Phosphorus 12X, Physostigma Venenosum 12X, Staphysagria 12X, Symphytum Officinale 6X, Vaccinium Myrtillus 6X, 12X, 30X.
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PURPOSE:
Allium Cepa – Eye Support, Apis Mellifica – Allergy of the Eye, Argentum Nitricum – Blurred Vision, Calcarea Fluorica – Double
Vision, Carboneum Sulphuratum – Eye Dryness, Cedron – Eye Itching, Eye (Suis) – Eye Support, Gelsemium Sempervirens - Lachrymation, Kali Iodatum – Eye Pain, Nux Moschata – Eye Dryness, Phosphorus - Photophobia, Physostigma Venenosum – Eye Redness, Staphysagria – Allergy of the Eye, Symphytum Officinale – Eye Injury, Vaccinium Myrtillus – Blurred Vision. -
INDICATIONS:
• For the temporary relief of symptoms including:
• eye support • allergy of the eye • blurred vision
• double vision • eye dryness • eye itching
• lachrymation • eye pain • Photophobia
• eye redness • eye injury
These statements are based upon homeopathic principles. They have not been reviewed by the Food and Drug Administration.
- WARNINGS:
- KEEP OUT OF REACH OF CHILDREN:
- DIRECTIONS:
- INACTIVE INGREDIENTS:
- QUESTIONS:
- PACKAGE LABEL DISPLAY:
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INGREDIENTS AND APPEARANCE
EYE SUPPORT
allium cepa, symphytum officinale, argentum nitricum, eye (suis), vaccinium myrtillus, apis mellifica, calcarea fluorica, carboneum sulphuratum, cedron, gelsemium sempervirens, kali iodatum, nux moschata, phosphorus, physostigma venenosum, staphysagria liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:43742-2083 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ONION (UNII: 492225Q21H) (ONION - UNII:492225Q21H) ONION 6 [hp_X] in 1 mL COMFREY ROOT (UNII: M9VVZ08EKQ) (COMFREY ROOT - UNII:M9VVZ08EKQ) COMFREY ROOT 6 [hp_X] in 1 mL SILVER NITRATE (UNII: 95IT3W8JZE) (SILVER CATION - UNII:57N7B0K90A) SILVER NITRATE 6 [hp_X] in 1 mL SUS SCROFA EYE (UNII: X3AOK514E6) (SUS SCROFA EYE - UNII:X3AOK514E6) SUS SCROFA EYE 6 [hp_X] in 1 mL BILBERRY (UNII: 9P2U39H18W) (BILBERRY - UNII:9P2U39H18W) BILBERRY 6 [hp_X] in 1 mL APIS MELLIFERA (UNII: 7S82P3R43Z) (APIS MELLIFERA - UNII:7S82P3R43Z) APIS MELLIFERA 12 [hp_X] in 1 mL CALCIUM FLUORIDE (UNII: O3B55K4YKI) (FLUORIDE ION - UNII:Q80VPU408O) CALCIUM FLUORIDE 12 [hp_X] in 1 mL CARBON DISULFIDE (UNII: S54S8B99E8) (CARBON DISULFIDE - UNII:S54S8B99E8) CARBON DISULFIDE 12 [hp_X] in 1 mL HOMALOLEPIS CEDRON SEED (UNII: KHI40967MV) (HOMALOLEPIS CEDRON SEED - UNII:KHI40967MV) HOMALOLEPIS CEDRON SEED 12 [hp_X] in 1 mL GELSEMIUM SEMPERVIRENS ROOT (UNII: 639KR60Q1Q) (GELSEMIUM SEMPERVIRENS ROOT - UNII:639KR60Q1Q) GELSEMIUM SEMPERVIRENS ROOT 12 [hp_X] in 1 mL POTASSIUM IODIDE (UNII: 1C4QK22F9J) (IODIDE ION - UNII:09G4I6V86Q) IODIDE ION 12 [hp_X] in 1 mL NUTMEG (UNII: AEE24M3MQ9) (NUTMEG - UNII:AEE24M3MQ9) NUTMEG 12 [hp_X] in 1 mL PHOSPHORUS (UNII: 27YLU75U4W) (PHOSPHORUS - UNII:27YLU75U4W) PHOSPHORUS 12 [hp_X] in 1 mL PHYSOSTIGMA VENENOSUM SEED (UNII: CJV9E9IIOA) (PHYSOSTIGMA VENENOSUM SEED - UNII:CJV9E9IIOA) PHYSOSTIGMA VENENOSUM SEED 12 [hp_X] in 1 mL DELPHINIUM STAPHISAGRIA SEED (UNII: 00543AP1JV) (DELPHINIUM STAPHISAGRIA SEED - UNII:00543AP1JV) DELPHINIUM STAPHISAGRIA SEED 12 [hp_X] in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) ALCOHOL (UNII: 3K9958V90M) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:43742-2083-1 30 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product 05/09/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 05/09/2023 Labeler - Deseret Biologicals, Inc. (940741853) Registrant - Apotheca Company (844330915) Establishment Name Address ID/FEI Business Operations Apotheca Company 844330915 manufacture(43742-2083) , api manufacture(43742-2083) , label(43742-2083) , pack(43742-2083)
