All Natural Eye Patch

Manufacturer
Tianjin Oculax Biotech Inc
Effective date
2023-12-26
Label type
HUMAN OTC DRUG LABEL
Version
32884
Source
full-release
Hydrated at
2026-06-01 00:05:44

Label at a glance#

ProductAll Natural Eye Patch
Active ingredientMENTHOL
Label structure15 sections

Indications and uses

For the temporary relief of minor aches and pains of the eyes.

Dosage and administration

Adults and children 6 years of age and older: Apply patches to areas as diagram shown. Remove after 8 hours. Children 2 to 6 years of age and adults with compromised health: Use only under the guidance of a doctor. Children under 2 years of age: Do not use, consult a doctor. Refer to the above warnings: use otherwise than as directed.

Storage and handling

Use immediately after individual package is opened. Store below 35 ℃ (95 ℉) in a dry area.

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

Menthol       2.5%

PURPOSE

OTC - PURPOSE SECTION

Menthol         External Analgesic

USES

INDICATIONS & USAGE SECTION

For the temporary relief of minor aches and pains of the eyes.

Warnings

WARNINGS SECTION

For External Use only.

Do not use

OTC - DO NOT USE SECTION

on wounds.
on irritated or damaged skin.
if the appearance of this product has changed.
if you are hypersensitive to this product.
otherwise than as directed.

Ask a Doctor or Pharmacist Before Use If you are

OTC - ASK DOCTOR/PHARMACIST SECTION

pregnant.
taking other medications.

When using this product

OTC - WHEN USING SECTION

avoid contact with the eye or mucous membranes.
supervise use by children.
use caution if prone to allergic reactions.

Stop Use and Ask a Doctor If

OTC - STOP USE SECTION

condition worsens.
symptoms persist for more than 7 days.
symptoms clear up and occur again within a few days.
excessive irritation of the skin develops.
redness is present.

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.

Directions

DOSAGE & ADMINISTRATION SECTION

Adults and children 6 years of age and older: Apply patches to areas as diagram shown. Remove after 8 hours. Children 2 to 6 years of age and adults with compromised health: Use only under the guidance of a doctor. Children under 2 years of age: Do not use, consult a doctor. Refer to the above warnings: use otherwise than as directed.

Other Information

STORAGE AND HANDLING SECTION

Use immediately after individual package is opened.
Store below 35 ℃ (95 ℉) in a dry area.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

GLYCERIN, LIGUSTICUM WALLICHII ROOT, SALVIA MILTIORRHIZA ROOT, CHRYSANTHEMUM INDICUM FLOWER, LAVANDULA ANGUSTIFOLIA FLOWER, ANGELICA ARCHANGELICA ROOT

Questions or Comments?

OTC - QUESTIONS SECTION

3T Herbtech Inc.
(800)668-8922
mfg3t@3t-herb.com

Manufactured byTianjin Oculax Biotech Inc 6 Ziyuan Road, B201 Huayuan Domain DistrictTianjin 300131, China

SPL UNCLASSIFIED SECTION

Distributed by

3T Herbtech Inc.
1720 S. San Gabriel Blvd, Suite 111
San Gabriel, CA 91776 USA

Drug Facts

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
2056513menthol 2.5 % Medicated PatchPSN32884
2056513menthol 0.025 MG/MG Medicated PatchSCD32884
2056513menthol 2.5 % Medicated PatchSY32884

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72455-001-05All Natural Eye Patch30 in 1 BOXPATCH3032884
72455-001-05All Natural Eye Patch24 mg in 1 PATCHPATCH2432884
72455-001-10All Natural Eye Patch60 in 1 BOXPATCH6032884
72455-001-20All Natural Eye Patch120 in 1 BOXPATCH12032884

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
72455-001ALL NATURAL EYE PATCH (MENTHOL) PATCH [TIANJIN OCULAX BIOTECH INC]32884Legacy NDC, 4 package rows20231227_db7446aa-442e-4fbd-bb0f-b330713c5666.zip

Products#

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

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

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72455-00172455-001-05, 72455-001-10, 72455-001-20

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 · Source PDF

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
5d6e19ca-3038-4b69-8aa7-e4e03fe8da98db7446aa-442e-4fbd-bb0f-b330713c56662023-12-26WarningsExact identifier
spl id: 5d6e19ca-3038-4b69-8aa7-e4e03fe8da98
spl set id: db7446aa-442e-4fbd-bb0f-b330713c5666

Reported adverse events (FAERS/openFDA)#

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