Aging Eye Relief

Manufacturer
Similasan AG
Effective date
2021-10-28
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-06-01 02:19:18

Label at a glance#

ProductAging Eye Relief
Active ingredientJACOBAEA MARITIMA, SODIUM CHLORIDE, RUTA GRAVEOLENS FLOWERING TOP
Label structure13 sections

Indications and uses

According to homeopathic principles, the active ingredients in this medication help temporarily relieve minor symptoms such as: Blurred vision Eyestrain Tearing due to dryness

Dosage and administration

Remove tamper-evident seal from neck of bottle. Twist cap off bottle. DON’T squeeze bottle, squeeze plastic tip to release 1 to 2 drops into eye. Apply every 3-4 hours, or as directed by a doctor. Replace cap after each use.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Cineraria maritima 6X

Purpose

OTC - PURPOSE SECTION

Blurred vision

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Natrium muriaticum 6X      

Purpose

OTC - PURPOSE SECTION

burning, reflex tearing due to dryness, eyestrain, corneal opacity, sensitivity to light

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ruta graveolens 6X      

Purpose

OTC - PURPOSE SECTION

eyestrain, rednesss, eye pain when reading

Uses:

INDICATIONS & USAGE SECTION

According to homeopathic principles, the active ingredients in this medication help temporarily relieve minor symptoms such as:

  • Blurred vision
  • Eyestrain
  • Tearing due to dryness

Warnings:

WARNINGS SECTION

  • 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 container to any surface.
  • To avoid contamination, use within 30 days of opening. Expiration date only refers to unopened bottle.
  • †Our drops will not harm contact lenses, however we recommend not wearing contacts while experiencing eye irritation.

If pregnant, trying to get pregnant or breast feeding,

OTC - PREGNANCY OR BREAST FEEDING SECTION

ask a health professional before use.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away.

Do not use:

OTC - DO NOT USE SECTION

  • if the solution changes color or becomes cloudy.

Stop use and ask a doctor if:

OTC - STOP USE SECTION

  • symptoms worsen or persist for more than 72 hours
  • you experience eye pain or changes in vision

Directions:

DOSAGE & ADMINISTRATION SECTION

  • Remove tamper-evident seal from neck of bottle.
  • Twist cap off bottle.
  • DON’T squeeze bottle, squeeze plastic tip to release 1 to 2 drops into eye.
  • Apply every 3-4 hours, or as directed by a doctor.
  • Replace cap after each use.

Other Information:

OTHER SAFETY INFORMATION

Active ingredients are manufactured according to homeopathic principles.

Inactive Ingredients:

INACTIVE INGREDIENT SECTION

Borate buffer, Purified water, Silver sulphate (as preservative), Sodium nitrate

Questions?

OTC - QUESTIONS SECTION

Reach our representatives at 1-800-240-9780 or getinfo@similasanusa.com.
www.SimilasanUSA.com

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Similasan
Aging Eye Relief

STERILE EYE DROPS

10 ml / 0.33
fl oz

PRINCIPAL DISPLAY PANEL Similasan Aging Eye Relief STERILE EYE DROPS 10 ml / 0.33 fl ozPRINCIPAL DISPLAY PANEL Similasan Aging Eye Relief STERILE EYE DROPS 10 ml / 0.33 fl oz

PRINCIPAL DISPLAY PANEL Similasan Aging Eye Relief STERILE EYE DROPS 10 ml / 0.33 fl ozPRINCIPAL DISPLAY PANEL Similasan Aging Eye Relief STERILE EYE DROPS 10 ml / 0.33 fl oz

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
30b0ac6e-02aa-0e5c-0d8b-cffdf3a282b2Product name520250304
bed0530e-f939-4541-956b-6928a2f6404fProduct name120241008
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362d7abb-94e6-4c60-9a58-266894157713Product name120231023
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e4870509-7e28-6f92-f0be-dd3dd889a9cfProduct name520200810
6e9d4a47-c464-b93e-aebc-ad7bffc9c4cdProduct name220190619
444b3e50-f226-46ef-bfca-2e7035d140cdProduct name120190611
816b97af-edc5-4060-aff1-b814bdbcad50Product name120190415
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
cefa60e2-a5b5-493e-9c54-24735b7dc509Product name220171212
419aab54-5d5a-4146-9453-026d4a9991beProduct name220170525
d5e51f11-ad28-caa4-4b49-4143974782adProduct name120150831
290f523a-f9db-9774-b5a9-e1f908ac1782Product name120150828
0ca1d589-929b-4b33-bc5b-1d84abdafa6aProduct name120150324
fc363c46-397b-4476-ac0f-70e43e8e4592Product name120150324
89dac932-b90a-4410-9ab1-84c53e57de25Product name120150316
5668b646-cd56-c3c7-bdea-3f6b1a8840dbProduct name120140508
684ea482-2e8b-14af-5664-b98f1e402036Product name120140508
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8dbefedf-0a0d-a224-5a3c-66dc9e11c2ddProduct name120140508
b060cc1a-fe47-856b-0b77-4448b5963de8Product name120140508
c6b65c52-69c7-df49-550a-a50c137f6218Product name120140508
ec2149b3-5c6d-5344-f757-c86411073075Product name120140508
ed912195-5da0-0f2f-6f4b-3ef17710cbe3Product name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
53799-360-112025-01-30C16284748780-12cef2736-6e3c-d83d-e063-dadaa90ab31fAging Eye Relief

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
53799-360-11Aging Eye Relief10 mL in 1 BOTTLE, DROPPERSOLUTION/ DROPS104
53799-360-11Aging Eye Relief1 in 1 BOXSOLUTION/ DROPS14

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
53799-360AGING EYE RELIEF (JACOBAEA MARITIMA, SODIUM CHLORIDE AND RUTA GRAVEOLENS FLOWERING TOP) SOLUTION/ DROPS [SIMILASAN AG]4Legacy NDC, 2 package rows20230106_9371d46d-a957-467c-80fb-a4b0d2ccdd49.zip

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
53799-36053799-360-11

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 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
c005cbfd-1f01-4250-86b2-6a87100049f29371d46d-a957-467c-80fb-a4b0d2ccdd492021-10-28WarningsExact identifier
spl id: c005cbfd-1f01-4250-86b2-6a87100049f2
spl set id: 9371d46d-a957-467c-80fb-a4b0d2ccdd49

Reported adverse events (FAERS/openFDA)#

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