Hyaluronic Acid Micro
FDA Label NDC 70018-010

Full FDA labeling including Indications, Dosage, Usage, and Precautions

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Junmok International,inc for the product Hyaluronic Acid Micro (NDC 70018-010). 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 & usage, 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

Active Ingredient

Active Ingredient: Sodium hyaluronate 95.0%

Inactive Ingredient

Inactive Ingredient: Lactose

Purpose

Purpose: Skin Protectant

Warnings

Warnings: 1. Do not use if irritation occurs. 2. Avoid using on sensitive skin. 3. Keep out of reach of children 4. For external use only. 5. Store in a cool place

Keep Out Of Reach Of Children

Keep out of reach of babies and children

Indications & Usage

Indications & usage:1. Take a patch out of the pouch with dry hand after face washing. 2. Try not to touch the middle side (needle) and take off the protective film carefully. 3. Place and attach the middle side of the patch on a desired area vertically. 4. Press the middle part of the patch attached with fingers several times. 5. Go to bed with patch attached and take it off the next morning.

Dosage & Administration

Dosage & Administration: 2-3 times a week.

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