Tear Stimulation Forte

Manufacturer
Natural Ophthalmics, Inc
Effective date
2022-07-07
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 02:17:42

Label at a glance#

ProductTear Stimulation Forte
Active ingredientSODIUM CHLORIDE, ACONITUM NAPELLUS, EUPHRASIA STRICTA, ALUMINUM OXIDE, ARSENIC TRIOXIDE, NUTMEG, ZINC
Label structure12 sections

Indications and uses

According to homeopathic principles these drops are indicated for acute or chronic dry eyes, Sjögren’s or excessive watering secondary to dry eye.* * Claims are based on traditonal homeopathic practce, not accepted medical evidence. Not FDA evaluated.

Dosage and administration

Instill 1-3 drops in the eye. Use several times per day as needed.

Storage and handling

Safe Storage Room temperature 59 o to 86 o (15 o to 30 o C)

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Aconitum nap HPUS 15c
Alumina HPUS 14x
Arsenicum album HPUS 12x
Euphrasia (Eyebright) HPUS 5x
Nux mosch 6x
Nat mur 15c
Zincum met 11x

Uses

INDICATIONS & USAGE SECTION

According to homeopathic principles these drops are indicated for acute or chronic dry eyes, Sjögren’s or excessive watering secondary to dry eye.*


* Claims are based on traditonal homeopathic practce, not accepted medical evidence. Not FDA evaluated.

Directions

DOSAGE & ADMINISTRATION SECTION

Instill 1-3 drops in the eye. Use several times per day as needed.

Homeopathic Purpose

OTC - PURPOSE SECTION

  • Pulsatilla 8x }
  • Sepia 8x }
  • Euphrasia (Eyebright) 5x }
    • Alumina 10x } Dry eyes
  • Arsenicum album 12x }
  • Nux mosch 6x }
  • Zincum met 10x }

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Purified water
Sodium citrate

Sodium chloride

Polysorbate 80

Citric acid

Warnings

WARNINGS SECTION

For ophthalmic use.

Stop use and ask a doctor if

OTC - STOP USE SECTION

Stop use and ask a doctor if: You experience eye pain, changes in vision, continued redness or irritation of the eye. The condition worsens. Symptoms last longer than 72 hours.

Do not use

OTC - DO NOT USE SECTION

Do not use if solution becomes cloudy.

If pregnant or breast feeding

OTC - PREGNANCY OR BREAST FEEDING SECTION

If pregnant or breast feeding, ask a health professional before use.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. In case of accidental ingestion, get medical help or contact a Poison Control Center right away.

Storage

STORAGE AND HANDLING SECTION

  • Safe Storage

Room temperature
59 o to 86 o (15 o to 30 o C)

Label image

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL


LabelLabel

CartonCarton

DailyMed Product Concepts#

Product concept, Relation, Version table
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FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
68770-114-102024-01-30C16284748780-11030e365-1914-111a-e063-dadaa90a10e2Tear Stimulation Forte

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
68770-114-10Tear Stimulation Forte10 mL in 1 BOTTLE, DROPPERLIQUID102
68770-114-10Tear Stimulation Forte1 in 1 PACKAGELIQUID12

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
68770-114TEAR STIMULATION FORTE (ACONITUM NAPELLUS, NUTMEG, ARSENIC TRIOXIDE, ALUMINUM OXIDE, ZINC, EUPHRASIA STRICTA, SODIUM CHLORIDE) LIQUID [NATURAL OPHTHALMICS, INC]2Legacy NDC, 2 package rows20220709_c46d6f75-7ccf-3279-e053-2a95a90a1a39.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 14 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
68770-11468770-114-10

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 10 matching rows.

Source Document#

Source XML

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.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
e33ce1d6-f754-50fb-e053-2995a90ae6fac46d6f75-7ccf-3279-e053-2a95a90a1a392022-07-07WarningsExact identifier
spl id: e33ce1d6-f754-50fb-e053-2995a90ae6fa
spl set id: c46d6f75-7ccf-3279-e053-2a95a90a1a39

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.