Kopa Haiku Ringworm Treatment Cream

Manufacturer
Trovina Co. Ltd | Jiangxi Zhongletang Pharmaceuticals Co., Ltd.
Effective date
2026-06-30
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
weekly-update
Hydrated at
2026-07-17 21:41:56

Label at a glance#

ProductKopa Haiku Ringworm Treatment Cream
Active ingredientMICONAZOLE NITRATE
Label structure9 sections

Storage and handling

Store in a cool, dry environment.

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Miconazole nitrate 2%

OTC - PURPOSE SECTION

Antifungal

INDICATIONS & USAGE SECTION

For effective treatment of most athlete's foot (tinea pedis), jock itch (tinea cruris), and ringworm (tinea corporis).

Relieves itching, scaling, cracking, burning, redness, soreness, irritation, discomfort, and chafing associated with jock itch.

WARNINGS SECTION

For external use only.

OTC - DO NOT USE SECTION

on children under 2 years of age unless directed by a doctor.

OTHER SAFETY INFORMATION

avoid contact with the eyes.

OTC - STOP USE SECTION

Irritation occurs.

There is no improvement within 4 weeks for athlete's foot and ringworm.

There is no improvement within 2 weeks for jock itch.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

DOSAGE & ADMINISTRATION SECTION

■ clean the affected area and dry thoroughly ■ apply a thin layer of the product over affected area twice daily (morning and night) or as directed by a doctor ■ supervise children in the use of this product ■ for athlete's foot: pay special attention to spaces between the toes; wear well-fitting, ventilated shoes, and change shoes and socks at least once daily ■ for athlete's foot and ringworm, use daily for 4 weeks; for jock itch, use daily for 2 weeks ■ if condition persists longer, consult a doctor ■ this product is not effective on the scalp or nails

STORAGE AND HANDLING SECTION

Store in a cool, dry environment.

INACTIVE INGREDIENT SECTION

Aqua (Water), Melaleuca Alternifolia (Tea Tree) Leaf Oil, Lavandula Angustifolia (Lavender) Oil, Eugenia Caryophyllus (Clove) Leaf Oil/Bud Oil, Aloe Barbadensis Leaf Extract, Glycyrrhiza Glabra (Licorice) Root Extract, Chamomilla Recutita (Matricaria) Flower Extract, Eucalyptus Globulus Leaf Oil, Macadamia Seed Oil, Safflower Seed Oil, Olive Fruit Oil, Avocado Oil, Sweet Almond Oil, Pumpkin Seed Oil, Geranium Flower Oil, Orange Peel Oil, Centella Asiatica / Cica, Tocopherol, Borneol, Menthol, Stearic Acid, Petrolatum, Paraffinum Liquidum, Glycerin, Triethanolamine.

OTC - QUESTIONS SECTION

Email at: service@kopahaiku.co.uk

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

ringwormringworm

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
ebc62596-fc97-4d03-9483-7ba095d25db7Product name120151210
3a55f4fb-5aec-4c88-0ff7-4d608ad4866aProduct name120140508
5b9a7965-36d2-8412-dcaf-f76a65411611Product name120140508

Products#

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

DailyMed product names page 1 of 1 · 29 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
87041-00887041-008-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 26 matching rows.

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
22026-06-23monthly-update2026-07-17 21:34:41
12026-05-27daily-update2026-06-04 05:10:14

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
Kopa Haiku Ringworm Treatment CreamMICONAZOLE NITRATE 2%Trovina Co. Ltd52cef8ec-6578-5e80-e063-6294a90ab4232026-06-30WarningsExact identifier
ndc (package): 87041-008-01
ndc (product): 87041-008
ndc11 (package): 87041000801
spl id: 5576dd76-d0f4-c042-e063-6294a90ad6d8
spl set id: 52cef8ec-6578-5e80-e063-6294a90ab423

Reported adverse events (FAERS/openFDA)#

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