Active Ingredient(S)
Pyrithione Zinc 2.0%
Zinc
FDA Label NDC 78565-007
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Meixin Beauty & Health Care Products Co., Ltd. for the product Zinc (NDC 78565-007). 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 active ingredient(s), purpose, warnings, do not use, otc - when using, otc - stop use, otc - keep out of reach of children, directions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Dandruff, Seborrheic dermatitis
Warnings
For external use only
Do Not Use
Avoid contact with eyes
Otc - When Using
When using this product Avoid contact with eyes. If contact occurs , rinse eyes thoroughly with water
Otc - Stop Use
Stop Use and Ask a Doctor if
Condition worsens or does not improve after regular use as directed
Otc - Keep Out Of Reach Of Children
Keep Out of Reach of Children
If swallowed , get medical help or contact a Poison Control Center right away
Directions
Use on affected areas in place of your regular soap.
For best results use at least twice a week or as directed by a doctor.
Work up a lather using warm water and massage into affected areas.
Rinse well.
Other Information
Store at room temperature
Inactive Ingredients
Sodium Palmitate , Sodium Palm Kernelate , Water , Glycerin ,Tetrasodium EDTA . Aloe Vera Extract
Indications & Usage
Controls , reduces , and helps stop the symptoms of dandruff and seborrheic dermatitis
Package Label - Principal Display Panel
120g 78565-007-01
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