Active Ingredient
Active ingredient: Allantoin 0.6%
Seuk
FDA Label NDC 54170-130
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Nanopoly Co., Ltd. for the product Seuk (NDC 54170-130). 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, inactive ingredient, purpose, warnings, keep out of reach of children, indications and usage, dosage and administration, 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
Inactive Ingredient
Inactive ingredients:
Coconut and Palm (Kernel/Oil), Jojoba Oil, Eriocephalus Punctulatus Oil, Phytosqualane, Grape Seed Oil, Tea Tree Oil, Aloe Barbadensis Leaf Extract, Tocopherol, Oriental Herb Extract, Perfume, Colloidal Silver, Organic Germanium, Organic Selenium, Platinum
Purpose
Purpose: Skin Protectant
Warnings
Warnings: Don't use if redness or irritation occur.
Keep Out Of Reach Of Children
Keep out of reach of children: Keep out of reach of babies and children.
Indications And Usage
Indication and usage: Do not place a lot of water or moisture before and after use.
Dosage And Administration
Dosage and administration: Made enough foam with hands and rubbed on the face or body, and washing with water.
* Please review the disclaimer below.
