FDA.reportPublic FDA data

Aging Eye Relief

Manufacturer
Similasan Corporation
Effective date
2021-10-28
Label type
HUMAN OTC DRUG LABEL
Version
7
Source
full-release
Hydrated at
2026-06-01 02:19:58

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

NDC 59262-360-11
Similasan
Aging Eye Relief
STERILE EYE DROPS
10 ml / 0.33 fl oz

PRINCIPAL DISPLAY PANEL NDC 59262-360-11 Similasan Aging Eye Relief STERILE EYE DROPS 10 ml / 0.33 fl ozPRINCIPAL DISPLAY PANEL NDC 59262-360-11 Similasan Aging Eye Relief STERILE EYE DROPS 10 ml / 0.33 fl oz

PRINCIPAL DISPLAY PANEL NDC 59262-360-11 Similasan Aging Eye Relief STERILE EYE DROPS 10 ml / 0.33 fl ozPRINCIPAL DISPLAY PANEL NDC 59262-360-11 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
cefa60e2-a5b5-493e-9c54-24735b7dc509Product name620240814
362d7abb-94e6-4c60-9a58-266894157713Product name120231023
6bd95106-a412-1dad-b9cc-4cb74bfb27ceProduct name220230315
f1e0dc7e-7d61-4625-b6d9-4894927679d7Product name220211025
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
810ab97e-f109-f41c-7c83-6a652a9cbf43Product name120140508
87711080-88eb-65c5-b2dd-bf99e700a372Product name120140508
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
59262-360-112025-01-30C16284748780-12cef2736-88a3-d83d-e063-dadaa90ab31fAging Eye Relief

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
59262-360-11Aging Eye Relief10 mL in 1 BOTTLE, DROPPERSOLUTION/ DROPS107
59262-360-11Aging Eye Relief1 in 1 BOXSOLUTION/ DROPS17

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
59262-360AGING EYE RELIEF (JACOBAEA MARITIMA, SODIUM CHLORIDE AND RUTA GRAVEOLENS FLOWERING TOP) SOLUTION/ DROPS [SIMILASAN CORPORATION]7Legacy NDC, 2 package rows20230127_a5642552-fa6a-4245-8626-6561ae0a2d5c.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
59262-360-11ML - Milliliter59262-360b1a92b7d-3ea1-461c-a1f7-791ee056e70212022-06-06

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
JACOBAEA MARITIMAACTIVE INGREDIENTU4B223LS4X3
RUTA GRAVEOLENS FLOWERING TOPACTIVE INGREDIENTN94C2U587S3
SODIUM CHLORIDEACTIVE INGREDIENT451W47IQ8X3
CHLORIDE IONACTIVE MOIETYQ32ZN486983
JACOBAEA MARITIMAACTIVE MOIETYU4B223LS4X3
RUTA GRAVEOLENS FLOWERING TOPACTIVE MOIETYN94C2U587S3
BORIC ACIDINACTIVE INGREDIENTR57ZHV85D43
SILVER SULFATEINACTIVE INGREDIENT8QG6HV4ZPO3
SODIUM NITRATEINACTIVE INGREDIENT8M4L3H2ZVZ3
WATERINACTIVE INGREDIENT059QF0KO0R3

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
59262-36059262-360-11

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
NameUNIIKind
JACOBAEA MARITIMAU4B223LS4XACTIB
SODIUM CHLORIDE451W47IQ8XACTIB
RUTA GRAVEOLENS FLOWERING TOPN94C2U587SACTIB
BORIC ACIDR57ZHV85D4IACT
WATER059QF0KO0RIACT
SILVER SULFATE8QG6HV4ZPOIACT
SODIUM NITRATE8M4L3H2ZVZIACT

Source Document#

Source XML

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.

Inactive ingredient links page 1 of 1 · 18 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
BORIC ACIDBORIC ACIDR57ZHV85D4INJECTION, SOLUTION / INTRAVENOUS210 mgExact identifier — unii candidate
17 equally ranked IID candidates
BORIC ACIDBORIC ACIDR57ZHV85D4GEL / OPHTHALMIC0.5 %w/wExact identifier — unii candidate
17 equally ranked IID candidates
BORIC ACIDBORIC ACIDR57ZHV85D4SOLUTION / OPHTHALMIC60 mgExact identifier — unii candidate
17 equally ranked IID candidates
BORIC ACIDBORIC ACIDR57ZHV85D4EMULSION / OPHTHALMIC0.3 %w/vExact identifier — unii candidate
17 equally ranked IID candidates
BORIC ACIDBORIC ACIDR57ZHV85D4DROPS / OPHTHALMIC1 %w/wExact identifier — unii candidate
17 equally ranked IID candidates
BORIC ACIDBORIC ACIDR57ZHV85D4SUSPENSION / AURICULAR (OTIC)0.6 %w/vExact identifier — unii candidate
17 equally ranked IID candidates
BORIC ACIDBORIC ACIDR57ZHV85D4SHAMPOO / TOPICAL2 %w/wExact identifier — unii candidate
17 equally ranked IID candidates
SODIUM NITRATESODIUM NITRATE8M4L3H2ZVZSOLUTION / OPHTHALMIC1.18 %w/wExact identifier — unii candidate
BORIC ACIDBORIC ACIDR57ZHV85D4SOLUTION / AURICULAR (OTIC)0.05 %w/wExact identifier — unii candidate
17 equally ranked IID candidates
BORIC ACIDBORIC ACIDR57ZHV85D4SOLUTION, GEL FORMING, EXTENDED RELEASE / OPHTHALMIC0.3 %w/wExact identifier — unii candidate
17 equally ranked IID candidates
BORIC ACIDBORIC ACIDR57ZHV85D4EMULSION / TOPICAL1.3 %w/wExact identifier — unii candidate
17 equally ranked IID candidates
BORIC ACIDBORIC ACIDR57ZHV85D4MOUTHWASH / BUCCAL7.36 mg/1mlExact identifier — unii candidate
17 equally ranked IID candidates
BORIC ACIDBORIC ACIDR57ZHV85D4SUSPENSION/ DROPS / TOPICAL0.3 %w/vExact identifier — unii candidate
17 equally ranked IID candidates
BORIC ACIDBORIC ACIDR57ZHV85D4SOLUTION/ DROPS / OPHTHALMIC48 mgExact identifier — unii candidate
17 equally ranked IID candidates
BORIC ACIDBORIC ACIDR57ZHV85D4INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION / INTRAVENOUS0.53 %w/vExact identifier — unii candidate
17 equally ranked IID candidates
BORIC ACIDBORIC ACIDR57ZHV85D4SUSPENSION/ DROPS / AURICULAR (OTIC)3 mgExact identifier — unii candidate
17 equally ranked IID candidates
BORIC ACIDBORIC ACIDR57ZHV85D4JELLY / VAGINAL1 %w/wExact identifier — unii candidate
17 equally ranked IID candidates
BORIC ACIDBORIC ACIDR57ZHV85D4SUSPENSION/ DROPS / OPHTHALMIC22 mgExact identifier — unii candidate
17 equally ranked IID candidates

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
2c212019-a1e6-4fd0-9da9-a9d5b6e2d3f8a5642552-fa6a-4245-8626-6561ae0a2d5c2021-10-28WarningsExact identifier
spl id: 2c212019-a1e6-4fd0-9da9-a9d5b6e2d3f8
spl set id: a5642552-fa6a-4245-8626-6561ae0a2d5c

Reported adverse events (FAERS/openFDA)#

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