Dexamethasone Ointment

Manufacturer
Guangdong Quadrant Ecological Technology Co., Ltd.
Effective date
2025-10-15
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 01:39:04

Label at a glance#

ProductSeacall Dexamethasone Ointment.
Active ingredientDEXAMETHASONE
Label structure12 sections

Dosage and administration

1-2 times a day, take a small amount of application on the affected area and gently rub for a moment.

Storage and handling

If you are using other drugs, please consult your physician or pharmacist before using this product. Athletes should use it with caution. Sealed, stored in a cool place.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Dexamethasone 0.075%

Purpose

OTC - PURPOSE SECTION

Relief of dermatitis itching.

Use

INDICATIONS & USAGE SECTION

Used for pruritus, neurodermatitis, contact dermatitis, seborrheic dermatitis, chronic eczema.

Warnings

WARNINGS SECTION

For external use only.
Not for infants.
Use with caution in pregnant and lactating women.
Prohibited for those who are allergic to this product.
Allergic persons should be cautious.
Prohibit the use when the properties of the product have changed.
Should not be used on a large scale and for a long time.

Do not use

OTC - DO NOT USE SECTION

If the affected area has been broken, pus or obvious oozing or viral infections (such as herpes, blisters).

When Using

OTC - WHEN USING SECTION

Avoid contact with eyes, nose, and mouth. If contact occurs, rinse thoroughly with water.

Stop Use

OTC - STOP USE SECTION

Ask a doctor if any burning sensation, redness, or swelling at the site of application or bacterial or fungal infections occurs or if symptoms are not relieved after 1 week of use.

Keep Oot Of Reach Of Children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Children must be used under adult supervision. In case of accidental ingestion, get medical help or contact a poison control center immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

1-2 times a day, take a small amount of application on the affected area and gently rub for a moment.

Other information

STORAGE AND HANDLING SECTION

If you are using other drugs, please consult your physician or pharmacist before using this product.
Athletes should use it with caution.
Sealed, stored in a cool place.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Mineral Oil, Zinc Oxide, Beeswax, Copernicia Cerifera (Carnauba) Wax, Polyglyceryl-3 Diisostearate, Tocopheryl Acetate, Bisabolol, Octyldodecanol, Polyglyceryl-10 Dioleate, Borneol, Echium Plantagineum Seed Oil, Farnesol, Helianthus Annuus (Sunflower) Seed Oil Unsaponifiables, Zingiber Officinale (Ginger) Root Extract, Cardiospermum Halicacabum Flower/Leaf/Vine Extract, Tocopherol.

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

11

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
2691149dexAMETHasone 0.075 % Topical OintmentPSN3
2691149dexamethasone 0.00075 MG/MG Topical OintmentSCD3
2691149dexamethasone 0.075 % Topical OintmentSY3

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
DEXAMETHASONE Pharmacologic Class Indexing2Indexing - Pharmacologic Class20180813

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
1ea46721-9071-6b81-fd0a-a82bfbb014ecProduct name720250220
525701df-f985-480d-995a-e0ee70c2bdf4Product name520250128
ea50b939-d92a-4100-84f5-1c1089663837Product name220240705
941f67d9-7f03-56d2-750c-36de24f654dbProduct name320221117
d7d46a10-8766-d3c8-ebf2-2ccd9efdcae8Product name220220506
7b2c58e8-5850-4e3e-82e9-b1593b1de761Product name520220210
81e34474-b0a5-434f-8104-25d689efc99eProduct name120200303
05ab9c01-cd9a-4f59-b2e8-ddcb887cac39Product name120190408
0c7dba41-c919-5809-508d-4affe6cfcff2Product name220170817
399647c0-db89-02d1-991c-0c17b584482cProduct name120140508
3e9a6377-704f-dff7-b19f-56c98d40c444Product name120140508
4d2e6ff9-14f5-b84f-c39b-373b005712c1Product name120140508
725d71bf-f956-5cad-e556-fa39cb060dc8Product name120140508
9ea85abb-fa68-5da6-ab60-2c7eef579000Product name120140508
d029211e-5e6b-725f-3696-ac6ff77da222Product name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
76986-004-01Seacall Dexamethasone Ointment.20 g in 1 TUBEOINTMENT203

Products#

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

DailyMed product names page 1 of 1 · 19 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
76986-00476986-004-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 17 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
Seacall Dexamethasone Ointment.DEXAMETHASONE OINTMENTGuangdong Quadrant Ecological Technology Co., Ltd.201adf67-773c-34a2-e063-6394a90ac5252025-10-15WarningsExact identifier
ndc (package): 76986-004-01
ndc (product): 76986-004
ndc11 (package): 76986000401
spl id: 412fe0cc-0fac-234e-e063-6394a90a6c8c
spl set id: 201adf67-773c-34a2-e063-6394a90ac525

Reported adverse events (FAERS/openFDA)#

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