Dr.nuell Mugwort Shaking Pack
FDA Label NDC 73430-0002

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Apharm Co., Ltd. for the product Dr.nuell Mugwort Shaking Pack (NDC 73430-0002). 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, otc - purpose, otc - keep out of reach of children, indications & usage, warnings, inactive ingredient, 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

Otc - Active Ingredient

glycerin

Otc - Purpose

dual functionality for brightening and wrinkle improvement certified

Otc - Keep Out Of Reach Of Children

Keep out of reach of children

Indications & Usage

1. put 1st and 2nd packs in the pouch and seal them and shake them for 10 seconds

2. sweep the contents down and tear them along the bottom cut line

3. apply mixture to the fact with a sqag-hola and gently remove it from the bottom to the top after 20~30 minutes

4. remove the pack and apply skin product

Warnings

1) if there is any abnormal symptom or side effect, such as red spot, swelling and itching when using cosmetlcs or after using due to direct sunlight, consult dermatologists
2) Do not use for wounded areas
3) Precautions for storage and handling
keep out of reach of children, store away from direct sunlight
4) avoid the eye area

Inactive Ingredient

water, butylene glycol, 1,2-hexanediol, citric acid, etc

Dosage & Administration

For external use only

Package Label.Principal Display Panel

Label (Label)

Label (Label)

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