Smart Sunblock Puff

Manufacturer: EASY POWDER CO., LTD. | Kolmar Korea Co., Ltd.
Effective date: 2016-08-26
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: legacy-cache
Hydrated at: 2026-08-02 01:24:27

Label at a glance#

ProductSmart Sunblock Puff

Active ingredientZINC OXIDE, TITANIUM DIOXIDE

Label structure6 sections

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient: ZINC OXIDE 15.0%, TITANIUM DIOXIDE 10.2%

INACTIVE INGREDIENT

INACTIVE INGREDIENT SECTION

Inactive Ingredients: MICA, BISMUTH OXYCHLORIDE, SILICA, IRON OXIDES(CI 77492), 1,2-HEXANEDIOL, IRON OXIDES(CI 77491), IRON OXIDES(CI 77499), GLYCERYL CAPRYLATE, METHICONE

PURPOSE

OTC - PURPOSE SECTION

Purpose: Sunscreen

WARNINGS

WARNINGS SECTION

Warnings: For external use only Use only as directed Stop use and ask a doctor if rash or skin irritation occurs Do not use on damaged or broken skin When using this product, keep out of eyes. Rinse with water to remove Keep out of reach of children Store this product at room temperature

DESCRIPTION

DESCRIPTION SECTION

Indications & usage: Help protecting skin from UV-ray (SPF50+, PA+++) Help prevent and relieve chapped or cracked skin

Directions: Whenever UV-ray protection is needed or at the makeup finish stage, use the puff to spread powder gently over face. Apply in daily skin care routine

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of carton

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 7 matching rows.

Smart Sunblock Puff
ZINC OXIDE, TITANIUM DIOXIDE
ZINC OXIDE
ZINC CATION
TITANIUM DIOXIDE
MICA
BISMUTH OXYCHLORIDE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
69242-010	69242-010-01, 69242-010-02

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
ZINC OXIDE	SOI2LOH54Z	ACTIM
TITANIUM DIOXIDE	15FIX9V2JP	ACTIB
MICA	V8A1AW0880	IACT
BISMUTH OXYCHLORIDE	4ZR792I587	IACT

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
6bb6cad4-7476-4b8f-96f9-9e97eb854f7e			4d8cf4fb-ea47-459a-9288-78652ba1fb5b	2019-12-19	Warnings	Exact identifier spl set id: 4d8cf4fb-ea47-459a-9288-78652ba1fb5b

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.