Oheal Manuka Honey Eczema Cream

Manufacturer
Dr.luke Healthcare LLC
Effective date
2023-06-26
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 21:29:30

Label at a glance#

ProductOheal Manuka Honey Eczema Cream
Active ingredientCLOTRIMAZOLE
Label structure13 sections

Dosage and administration

1.Before using this product, wash and dry the affected area with warm water. 2.Apply an appropriate amount, and knead gently for two minutes to absorb it to achieve better results fully 2-3 times a day. 3.Use it for 3-5 days after symptoms disappear to prevent recurrence.

Storage and handling

If swallowed, rinse immediately with water, and get medical help or contact a poison control center right away.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Clotrimazole 1%

Purpose

OTC - PURPOSE SECTION

Antifungal

Use

INDICATIONS & USAGE SECTION

For Dermatitis, Psoriasis, Eczema, Rosacea, Shingles, Oily, Dry or Cracked Skin, General Skin Irritation, and more.

Warnings

WARNINGS SECTION

1. For external use only.
2. Stop using it and ask the doctor if you are allergic to this product.
3. Avoid contact with eyes, flush with water immediately if it gets into eyes.
4. If you are pregnant or breastfeeding, please don’t use it.
5. Keep out of reach of children.
6. Do not ingest.
7. Do not use if safety seal is broken or missing. Wash hands after use.

Do not use

OTC - DO NOT USE SECTION

If you are pregnant, breastfeeding
On children under 10 years
On unhealed wounds after surgery
If you are allergic to this product

Stop Use

OTC - STOP USE SECTION

You are experiencing severe allergic reactions, local ulcers, heavy rash, edema, or severe pain.

Ask Doctor

OTC - ASK DOCTOR SECTION

If you are allergic, feel unwell, please seek medical advice

Keep Oot Of Reach Of Children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Please do not allow unconscious persons to come into contact with.

Directions

DOSAGE & ADMINISTRATION SECTION

1.Before using this product, wash and dry the affected area with warm water.
2.Apply an appropriate amount, and knead gently for two minutes to absorb it to achieve better results fully 2-3 times a day.
3.Use it for 3-5 days after symptoms disappear to prevent recurrence.

Other information

STORAGE AND HANDLING SECTION

If swallowed, rinse immediately with water, and get medical help or contact a poison control center right away.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Rhinaca nthus Nasutus, HerbaViolae,
EeuphorbiaHir tall, Murrayaexotica L.,
Manthill1, Dryobala NopsSpp,
Sophora Flavescens, Manuka Honey,
CnidiumMonniericuss, ILAtin Title,
CortexDictamnil, Mosiacavaerieilev1,
RhizomaSmi Lacis alabrael, Phel,
lodendrn Amurenserupr1,
IFischereuphobiaR oot,
IGleditsiasinenesislinn1,
StemonaTuberosaLour.

PACKAGE LABEL.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

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Products#

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
83176-01183176-011-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 18 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
2764a99e-ce73-4d95-e063-6394a90a5475ff140a40-05ca-64bb-e053-6394a90a730d2024-11-20WarningsExact identifier
spl set id: ff140a40-05ca-64bb-e053-6394a90a730d

Reported adverse events (FAERS/openFDA)#

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