Dr.nuell Multi Sun Block
FDA Label NDC 73430-0005

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 Multi Sun Block (NDC 73430-0005). 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 - keep out of reach of children, indications & usage, warnings, inactive ingredient, dosage & administration, otc - purpose, 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

zinc oxide

Otc - Keep Out Of Reach Of Children

Keep out of reach of children

Indications & Usage

before foundation BB cream, apply it as a substitute for a primer.

if the foundation you use is dark, mix it with a small amount of sun block to adjust the tone before use

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, cyclopentasiloxane, etc.

Dosage & Administration

For external use only

Otc - Purpose

dual functionality for brightening and wrinkle improvement certified

mild UV protection without irritation SPF 42, PA+++

Package Label.Principal Display Panel

Label (Label)

Label (Label)

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