Oiangna Anti Fungal

Manufacturer
Guangzhou Huixue Biotechnology Co., Ltd.
Effective date
2025-12-22
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:28:33

Label at a glance#

ProductOiangna Anti Fungal
Active ingredientSALICYLIC ACID, SELENIUM SULFIDE
Label structure11 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Salicylic Acid 2%
Selenium sulfide 1%

INACTIVE INGREDIENT SECTION

Water (Aqua), Sodium Lauroyl Glutamate, Cocamidopropyl Betaine, Cetearyl Alcohol, Cocamidopropylamine Oxide, Sodium Chloride, PPG-3 Caprylyl Ether, Polyquaternium-10, Polyquaternium-47, Disodium EDTA, Citric Acid, Propylene Glycol, Sodium Cocamidopropyl PG-Dimonium Chloride Phosphate, Hexamidine Diisethionate, Phenoxyethanol, Ethylhexylglycerin, Aloe Barbadensis Leaf Juice, Rosmarinus Officinalis (Rosemary) Leaf Oil, Melaleuca Alternifolia(Tea Tree) Leaf Oil, Macadamia Ternifolia Seed Oil, Hydrolyzed Corn Starch, Coptis Chinensis Root Extract, Houttuynia Cordata Extract, Panax Ginseng Root Extract, Nymphaea Alba Flower Extract

OTC - PURPOSE SECTION

Antibacterial shampoo

INDICATIONS & USAGE SECTION

Helps reduce dandruff and control flaking Helps soothe scalp itching and irritation Helps restore scalp comfort and balance ·Leaves hair feeling fresh, clean, and healthy

WARNINGS SECTION

Warnings For external use only. Avoid contact with eyes. if contact occurs, rinse thoroughly with water. Stop use and ask a doctor if condition worsens or does not improve after regular use. Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away.

OTC - WHEN USING SECTION

1. Do not apply on other parts of the body, For topical use only on the scalp
2. Avoid contact with the eyes in case of accidental contact rinse eyes with large arnounts of cool tap water.

OTC - DO NOT USE SECTION

You have no family history of hair loss,hair loss is sudden and/or patchy
You do not know the reason for you hair loss.
You ae under 18 years of age, Do not use it on babies and children your scalp is red.inflamed.infected, irritated, or painful
You use other medicines on the scalp.Ask a doctor before use if you hace heart disease.

OTC - STOP USE SECTION

Chest pain, rapid heart beat, faintness, or dizziness occurs sudden, unexplained weight gain occurs,your hands or feet swell.

DOSAGE & ADMINISTRATION SECTION

Apply a small amount to wet hair and scalp. Gently massage into lather, leave on for 2-3 minutes. Rinse thoroughly. • Use 2-3 times per week or as needed.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Oiangna Anti-Fungal ShampooOiangna Anti-Fungal Shampoo

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
dea2eded-d1e7-46bb-9a3d-f8dc20de6277Product name120190408

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
87204-195-01Oiangna Anti Fungal300 mL in 1 BOTTLE, PLASTICSHAMPOO3001

Products#

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

DailyMed product names page 1 of 1 · 16 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
87204-19587204-195-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 14 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
Oiangna Anti FungalSELENIUM SULFIDE 1%Guangzhou Huixue Biotechnology Co., Ltd.468a7ca8-43c5-610f-e063-6294a90a07ac2025-12-22WarningsExact identifier
ndc (package): 87204-195-01
ndc (product): 87204-195
ndc11 (package): 87204019501
spl id: 468a7ca8-43c6-610f-e063-6294a90a07ac
spl set id: 468a7ca8-43c5-610f-e063-6294a90a07ac

Reported adverse events (FAERS/openFDA)#

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