Active Ingredient
Active ingredient: Allantoin 0.5%
Naaman
FDA Label NDC 61221-010
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Leader Green Co., Ltd. for the product Naaman (NDC 61221-010). 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: PONCIRUS TRIFOLIATA FRUIT, RED CLAY POWDER, NARINGINASE, LOBELIA SPICATA LEAF, MINERAL OIL, LIMONENE, (+)-, VITAMINE C, VINCAMINE
Purpose
Purpose: Skin Protectant
Warnings
Warnings:
1. In case of having following symptoms after using this, you're advised to stop using it immediately. If you keep using it, the symptoms will get worse and need to consult a dermatologist.
1) In case of having problems such as red rash, swollenness, itching, stimulation during usage.
2) In case of having the same symptoms above on the part you put this product on by direct sunlight.
2. You are banned to use it on the part where you have a scar, eczema, or dermatitis.
3. In case of getting it into your eyes, you have to wash it immediately.
Keep Out Of Reach Of Children
Keep out of reach of children:
Keep out of reach of babies and children
Indications And Usage
Indications and usage:
After basic skin care, apply adequate amount following the skin texture and gently tap to enhance absorption.
Dosage And Administration
Dosage and administration:
Take an adequate amount of this product.
* Please review the disclaimer below.
