Allergy Eye Relief

Manufacturer: Similasan AG
Effective date: 2020-10-07
Label type: HUMAN OTC DRUG LABEL
Version: 3
Source: full-release
Hydrated at: 2026-06-01 02:19:19

Label at a glance#

ProductAllergy Eye Relief

Active ingredientAPIS MELLIFERA, EUPHRASIA STRICTA, SCHOENOCAULON OFFICINALE SEED

Label structure10 sections

Indications and uses

According to homeopathic principles, the active ingredients in this product temporarily relieve minor symptoms such as: • itching • burning • excessive watering redness of eyes and lids

Dosage and administration

For adults and children age 2 and over: • remove a single-use dropper • twist flat end with ball to remove • squeeze plastic dropper to release 2-3 drops into eye and discard applicator • apply as needed • use a new dropper for every application

Contacts and useful links#

PhoneLabel contact1-800-240-9780

Websitewww.similasanusa.com

www.SimilasanUSA.com

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Apis mellifica 6X

Euphrasia officinalis (Eyebright) 6X

Sabadilla 6X

Purpose

OTC - PURPOSE SECTION

burning, itching, stinging

redness, swelling, watering

watering, redness of lids

Uses*

INDICATIONS & USAGE SECTION

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

• itching

• burning

• excessive watering

redness of eyes and lids

Warnings

WARNINGS SECTION

• For external use only.

• According to homeopathic principles, symptoms may temporarily worsen before improving (Initial exacerbation of symptoms).

• Use only if single-use dropper is intact.

• To avoid contamination, do not touch the tip of the dropper to any surface. Do not reuse. Once opened, discard.

• Contact lens wearers: consult a physician prior to using.

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

OTC - PREGNANCY OR BREAST FEEDING SECTION

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 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

For adults and children age 2 and over:

• remove a single-use dropper

• twist flat end with ball to remove

• squeeze plastic dropper to release 2-3 drops into eye and discard applicator

• apply as needed

• use a new dropper for every application

Other Information

OTHER SAFETY INFORMATION

Active ingredients are manufactured according to homeopathic principles.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Phosphate buffer, Purified water

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

Allergy Eye
Relief
0.4 ml/0.014 fl oz each

Allergy Eye Relief 0.4 ml/0.014 fl oz each

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
726062af-1135-4707-a1d7-57256991bbf9	Product name	2	20250226
19c71a3d-ed9c-166b-a7e5-38c250c35631	Product name	1	20140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
53799-302-12	2025-01-30	C162847	48780-1	2cef2736-6ca5-d83d-e063-dadaa90ab31f	Allergy Eye Relief Monodose

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
53799-302-12	Allergy Eye Relief	0.4 mL in 1 BOTTLE, DROPPER	SOLUTION/ DROPS	0.4		3

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
53799-302	ALLERGY EYE RELIEF (APIS MELLIFERA, EUPHRASIA STRICTA AND SCHOENOCAULON OFFICINALE SEED) SOLUTION/ DROPS [SIMILASAN AG]	3	Legacy NDC, 1 package rows	20230106_b81e6dd4-7936-4e97-bea9-194b7068b9e4.zip

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

Allergy Eye Relief
apis mellifera, euphrasia stricta and schoenocaulon officinale seed
APIS MELLIFERA
EUPHRASIA STRICTA
SCHOENOCAULON OFFICINALE SEED
WATER
SODIUM PHOSPHATE, MONOBASIC, DIHYDRATE
SODIUM PHOSPHATE, DIBASIC, ANHYDROUS

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
53799-302	53799-302-12

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
APIS MELLIFERA	7S82P3R43Z	ACTIB
EUPHRASIA STRICTA	C9642I91WL	ACTIB
SCHOENOCAULON OFFICINALE SEED	6NAF1689IO	ACTIB
WATER	059QF0KO0R	IACT
SODIUM PHOSPHATE, MONOBASIC, DIHYDRATE	5QWK665956	IACT
SODIUM PHOSPHATE, DIBASIC, ANHYDROUS	22ADO53M6F	IACT

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
0064fc96-86a7-4154-8ff1-d1744c015300			b81e6dd4-7936-4e97-bea9-194b7068b9e4	2020-10-07	Warnings	Exact identifier spl id: 0064fc96-86a7-4154-8ff1-d1744c015300 spl set id: b81e6dd4-7936-4e97-bea9-194b7068b9e4

Reported adverse events (FAERS/openFDA)#

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