EYE - CATARACT
- Manufacturer
- Natural Creations, Inc. | OHM Pharma, Inc.
- Effective date
- 2013-01-30
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 1
- Source
- full-release
- Hydrated at
- 2026-06-01 02:04:39
Label at a glance#
Contacts and useful links#
Label contents#
Full prescribing information#
OTC - ACTIVE INGREDIENT SECTION
ACTIVE INGREDIENTS (HPUS*): Euphrasia Officinalis 3X, Spigelia Anthelmia 3X, Vaccinium Myrtillus 3X, Arsenicum Album 12X, Calcarea Fluorica 12X, Causticum 12X, Gelsemium Sempervirens 12X, Magnesia Carbonica 12X, Mercurius Solubilis 12X, Osmium Metallicum 12X, Phosphorus 12X, Physostigma Venenosum 12X, Silicea 12X
OTC - PURPOSE SECTION
USES: Temporarily relieves pressive eye pain, eye redness, burning, flickering & sparks before eyes, lachrymation, eye fatigue &/or other symptoms related to eye cataracts.
INDICATIONS & USAGE SECTION
USES: Temporarily relieves pressive eye pain, eye redness, burning, flickering & sparks before eyes, lachrymation, eye fatigue &/or other symptoms related to eye cataracts.
DOSAGE & ADMINISTRATION SECTION
Directions: Adults & children above 12 years: 10 drops orally 3 times daily, or as directed by a health care professional.
OTC - KEEP OUT OF REACH OF CHILDREN SECTION
WARNINGS:
*Consult a physician for use in children under 12 years of age.
* IF PREGNANT OR BREAST-FEEDING, ask a health care professional before use.
* KEEP OUT OF THE REACH OF CHILDREN. In case of overdose (or accidental ingestion) get medical help or contact a Poison Control Center right away.
WARNINGS SECTION
WARNINGS:
*Consult a physician for use in children under 12 years of age.
* IF PREGNANT OR BREAST-FEEDING, ask a health care professional before use.
* KEEP OUT OF THE REACH OF CHILDREN. In case of overdose (or accidental ingestion) get medical help or contact a Poison Control Center right away.
INACTIVE INGREDIENT SECTION
Inactive Ingredients: Purified Water, USP Ethanol Alcohol 20%
OTC - DO NOT USE SECTION
Other Information: Tamper Seal: “Sealed for your protection.” Do not use if seal is broken or missing.
OTC - QUESTIONS SECTION
Questions & Comments? Natural Creations, Inc. / Woodbine, IA 51579 / 712.647.1600
*The letters “HPUS” indicate the components in the product are officially monographed in the Homeopathic Pharmacopeia of the United States.
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
NDC: 43406-0073-1
EYE - CATARACT
Cataracts & Eye Irritation
HOMEOPATHIC
1 fl oz (30 mL) 20% Alcohol
UPC: 877730001337
DailyMed Product Concepts#
| Product concept | Relation | Version | Effective |
|---|---|---|---|
| 63f39a63-5cd1-4016-bd86-2bbb0f6c3139 | Product name | 3 | 20240506 |
| e5a77e9c-c528-733a-173d-914a234c024b | Product name | 5 | 20240506 |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 43406-0073-1 | 2019-11-27 | C162847 | 48780-1 | 9855d018-d4d2-cd31-e053-dbdaa90ab51a | EYE - CATARACT |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 43406-0073-1 | EYE - CATARACT | 30 mL in 1 BOTTLE, DROPPER | LIQUID | 30 | 1 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 43406-0073 | EYE - CATARACT (EUPHRASIA STRICTA, SPIGELIA ANTHELMIA, BILBERRY, ARSENIC TRIOXIDE, CALCIUM FLUORIDE, CAUSTICUM, GELSEMIUM SEMPERVIRENS ROOT, MAGNESIUM CARBONATE, MERCURIUS SOLUBILIS, OSMIUM, PHOSPHORUS, PHYSOSTIGMA VENENOSUM SEED , SILICON DIOXIDE) LIQUID [NATURAL CREATIONS, INC.] | 1 | Legacy NDC, 1 package rows | 20130520_47907adc-672e-4ff7-9bcb-3bc9168339b1.zip |
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | SPL version | Uploaded |
|---|---|---|---|---|
| ARSENIC TRIOXIDE | ACTIVE INGREDIENT | S7V92P67HO | 1 | |
| BILBERRY | ACTIVE INGREDIENT | 9P2U39H18W | 1 | |
| CALCIUM FLUORIDE | ACTIVE INGREDIENT | O3B55K4YKI | 1 | |
| CAUSTICUM | ACTIVE INGREDIENT | DD5FO1WKFU | 1 | |
| EUPHRASIA STRICTA | ACTIVE INGREDIENT | C9642I91WL | 1 | |
| GELSEMIUM SEMPERVIRENS ROOT | ACTIVE INGREDIENT | 639KR60Q1Q | 1 | |
| MAGNESIUM CARBONATE | ACTIVE INGREDIENT | 0E53J927NA | 1 | |
| MERCURIUS SOLUBILIS | ACTIVE INGREDIENT | 324Y4038G2 | 1 | |
| OSMIUM | ACTIVE INGREDIENT | 2E7M255OPY | 1 | |
| PHOSPHORUS | ACTIVE INGREDIENT | 27YLU75U4W | 1 | |
| PHYSOSTIGMA VENENOSUM SEED | ACTIVE INGREDIENT | CJV9E9IIOA | 1 | |
| SILICON DIOXIDE | ACTIVE INGREDIENT | ETJ7Z6XBU4 | 1 | |
| SPIGELIA ANTHELMIA | ACTIVE INGREDIENT | WYT05213GE | 1 | |
| ARSENIC CATION (3+) | ACTIVE MOIETY | C96613F5AV | 1 | |
| BILBERRY | ACTIVE MOIETY | 9P2U39H18W | 1 | |
| CARBONATE ION | ACTIVE MOIETY | 7UJQ5OPE7D | 1 | |
| CAUSTICUM | ACTIVE MOIETY | DD5FO1WKFU | 1 | |
| COLLOIDAL SILICON DIOXIDE | ACTIVE MOIETY | ETJ7Z6XBU4 | 1 | |
| EUPHRASIA STRICTA | ACTIVE MOIETY | C9642I91WL | 1 | |
| FLUORIDE ION | ACTIVE MOIETY | Q80VPU408O | 1 | |
| GELSEMIUM SEMPERVIRENS ROOT | ACTIVE MOIETY | 639KR60Q1Q | 1 | |
| MERCURIUS SOLUBILIS | ACTIVE MOIETY | 324Y4038G2 | 1 | |
| OSMIUM | ACTIVE MOIETY | 2E7M255OPY | 1 | |
| PHOSPHORUS | ACTIVE MOIETY | 27YLU75U4W | 1 | |
| PHYSOSTIGMA VENENOSUM SEED | ACTIVE MOIETY | CJV9E9IIOA | 1 | |
| SPIGELIA ANTHELMIA | ACTIVE MOIETY | WYT05213GE | 1 | |
| ALCOHOL | INACTIVE INGREDIENT | 3K9958V90M | 1 | |
| WATER | INACTIVE INGREDIENT | 059QF0KO0R | 1 |
Products#
Every source-derived product name is available through these pages.
- EYE - CATARACT
- Euphrasia Stricta, Spigelia Anthelmia, Bilberry, Arsenic Trioxide, Calcium Fluoride, Causticum, Gelsemium Sempervirens Root, Magnesium Carbonate, Mercurius Solubilis, Osmium, Phosphorus, Physostigma Venenosum Seed , Silicon Dioxide
- EUPHRASIA STRICTA
- SPIGELIA ANTHELMIA
- BILBERRY
- ARSENIC TRIOXIDE
- ARSENIC CATION (3+)
- CALCIUM FLUORIDE
- FLUORIDE ION
- CAUSTICUM
- GELSEMIUM SEMPERVIRENS ROOT
- MAGNESIUM CARBONATE
- CARBONATE ION
- MERCURIUS SOLUBILIS
- OSMIUM
- PHOSPHORUS
- PHYSOSTIGMA VENENOSUM SEED
- SILICON DIOXIDE
- COLLOIDAL SILICON DIOXIDE
- WATER
- ALCOHOL
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 43406-0073 | 43406-0073-1 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| EUPHRASIA STRICTA | C9642I91WL | ACTIB |
| SPIGELIA ANTHELMIA | WYT05213GE | ACTIB |
| BILBERRY | 9P2U39H18W | ACTIB |
| ARSENIC TRIOXIDE | S7V92P67HO | ACTIM |
| CALCIUM FLUORIDE | O3B55K4YKI | ACTIB |
| CAUSTICUM | DD5FO1WKFU | ACTIB |
| GELSEMIUM SEMPERVIRENS ROOT | 639KR60Q1Q | ACTIB |
| MAGNESIUM CARBONATE | 0E53J927NA | ACTIB |
| MERCURIUS SOLUBILIS | 324Y4038G2 | ACTIB |
| OSMIUM | 2E7M255OPY | ACTIB |
| PHOSPHORUS | 27YLU75U4W | ACTIB |
| PHYSOSTIGMA VENENOSUM SEED | CJV9E9IIOA | ACTIB |
| SILICON DIOXIDE | ETJ7Z6XBU4 | ACTIB |
| WATER | 059QF0KO0R | IACT |
| ALCOHOL | 3K9958V90M | IACT |
Source Document#
Inactive ingredient matches#
Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.
| DailyMed ingredient | IID ingredient | UNII | Dosage form / route | Potency | Maximum daily exposure | Match |
|---|---|---|---|---|---|---|
| ALCOHOL | ALCOHOL | 3K9958V90M | SOLUTION / INTRAVENOUS | 99 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | INJECTION, SOLUTION / SUBCUTANEOUS | 6.1 %v/v | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SOLUTION / RESPIRATORY (INHALATION) | 0.08 %w/v | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SPRAY / SUBLINGUAL | 397 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SOLUTION / TOPICAL | 2445 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | GEL / DENTAL | 1.8 %w/w | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | AEROSOL, FOAM / TOPICAL | 4504 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | AEROSOL / NASAL | 20 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | AEROSOL, SPRAY / TOPICAL | 561 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | INJECTION / INTRAMUSCULAR | 1491 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SOLUTION / INTRAVESICAL | 7892 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | LIQUID / INTRAMUSCULAR | 400 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SPRAY / TRANSDERMAL | 90 %w/v | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | DROPS / ORAL | 210 mg/1ml | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SUSPENSION / ORAL | 681 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | LIQUID / INTRAVENOUS | 400 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SUSPENSION / RECTAL | 0.35 %v/v | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | TABLET, DELAYED RELEASE / ORAL | NA | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | DROPS / NASAL | 10 mg/1ml | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | INJECTION, EMULSION / INTRAVENOUS | 520 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | LOTION / TOPICAL | 25 %w/w | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | GEL / RECTAL | 898 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SOLUTION, CONCENTRATE / INTRAVENOUS | 4000 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | PASTE / DENTAL | 1.8 %w/w | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | GEL, METERED / TRANSDERMAL | 3675 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | AEROSOL, METERED / NASAL | 70 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | INJECTION / INTRAVASCULAR | 100 %v/v | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SYRUP / ORAL | 21000 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | INJECTION / SUBCUTANEOUS | 149 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | AEROSOL, SPRAY / RESPIRATORY (INHALATION) | 35.75 %w/w | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | CONCENTRATE / BUCCAL | 679 mg/1ml | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | INJECTION / INTRAVENOUS | 92 %w/v | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | CONCENTRATE / ORAL | 198 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SOLUTION / TRANSDERMAL | 49.37 %w/v | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SPRAY, METERED / SUBLINGUAL | 29 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SWAB / TOPICAL | 2250 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | ELIXIR / ORAL | 13675 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | GEL, METERED / TOPICAL | 541 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SOLUTION / OPHTHALMIC | 0.5 %w/v | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | POWDER, FOR SOLUTION / TOPICAL | 40 %w/w | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | GEL / TOPICAL | 9971 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | AEROSOL, METERED / RESPIRATORY (INHALATION) | 26664 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | CAPSULE / ORAL | 882 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | LIQUID / RESPIRATORY (INHALATION) | 5 %w/w | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | INJECTION, SOLUTION / INTRAMUSCULAR | 1000 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | MOUTHWASH / BUCCAL | 200 mg/1ml | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SPRAY / TOPICAL | 3633 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | INJECTION, SOLUTION / INTRAVENOUS | 6405 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | LIQUID / ORAL | 3563 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | JELLY / VAGINAL | NA | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SOLUTION, CONCENTRATE / ORAL | 150.68 mg/1ml | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | CAPSULE, EXTENDED RELEASE / ORAL | 8 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | GEL / TRANSDERMAL | 7360 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SOLUTION / DENTAL | 12.8 %w/w | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SPRAY / NASAL | 20 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SOLUTION / NASAL | 10 mg/1ml | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SOLUTION / ORAL | 6624 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | AEROSOL / TOPICAL | 561 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SHAMPOO / TOPICAL | 714 mg |
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| c8d4ff50-4e6c-4d09-964c-dfdea85ca072 | 47907adc-672e-4ff7-9bcb-3bc9168339b1 | 2013-01-30 | Warnings | c8d4ff50-4e6c-4d09-964c-dfdea85ca072 47907adc-672e-4ff7-9bcb-3bc9168339b1 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
