Otc - Active Ingredient
Active Ingredient Purpose
Zinc Pyrithione 1% Anti-dandruff
Halsa Anti Dandruff
FDA Label NDC 40104-380
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Ningbo Pulisi Daily Chemical Products Co., Ltd. for the product Halsa Anti Dandruff (NDC 40104-380). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding otc - active ingredient, otc - purpose, otc - keep out of reach of children, indications & usage, warnings, dosage & administration, inactive ingredient, package label.principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Otc - Purpose
helps prevent recumence of flaking and itching associated with dandruff
Otc - Keep Out Of Reach Of Children
If swallowed, get medical help or contact a Poison Control Center right away.
Do not get into eyes, if contact occurs, rinse eyes thoroughly with water.
Indications & Usage
Shake well, wet hair, massage onto scalp. Rinse, repeat if desired.
For best results, use at least twice a week or as directed.
For maximum dandruff control, use every time you shampoo.
Warnings
For external use only.
Stop use and ask a doctor if Condition worsens or if symptoms persist.
Dosage & Administration
shake well, wet hair, massage onto scalp, rinse, repeat if desired.
Inactive Ingredient
water, sodium laureth sulfate, cocamide DEA, cocamidopropyl betaine, sodium Chloride, Glycerin, Fragrance, citric acid, tetrasodium EDTA, DMDM hydantoin.
* Please review the disclaimer below.
