Otc - Active Ingredient
Niacinamide, Adenosine
Dr. Sunmi Care Duel Hyaluronic Acid Essence Liquid
FDA Label NDC 82083-0020
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Laon Commerce Co Ltd for the product Dr. Sunmi Care Duel Hyaluronic Acid Essence (NDC 82083-0020). 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, inactive ingredient, otc - purpose, otc - keep out of reach of children, indications & usage, warnings, dosage & 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
Water
Panthenol
Folic Acid
1,2-Hexanediol
Sodium Hyaluronate
Ethylhexylglycerin
Otc - Purpose
skin protect
Otc - Keep Out Of Reach Of Children
KEEP OUT OF REACH OF THE CHILDREN
Indications & Usage
Take an appropriate amount of essence and gently spread over the entire face for absorption.
Warnings
2. Precautions when using
1) When using cosmetics or after use, if there are any abnormal
symptoms or side effects such as red spots, swelling or itching
in the area of u se due to direct sunlight, consult with a specialist.
2) Refrain from using on areas with scars. 3) Precautions for sto
rage and handling A) Keep out of reach of children B) Keep away
from direct sunlight.
Dosage & Administration
topical use only
Package Label.Principal Display Panel
1 (Label Box)
* Please review the disclaimer below.
