UV defense me. No sebum sun cream

Manufacturer
Magnif Co., Ltd | Korea Kolmar Co. Ltd
Effective date
2024-07-18
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-06-01 00:15:38

Label at a glance#

ProductUV defense me. No sebum sunscreen
Active ingredientZINC OXIDE
Label structure8 sections

Indications and uses

helps prevent sunburn if used as directed with other sun protection measures (see Directions), decreases the risk of skin cancer and early skin aging caused by the sun

Dosage and administration

For sunscreen use: apply liberally 15 minutes before sun exposure reapply at least every 2 hours use a water-resistant sunscreen if swimming or sweating Sun Protection Measures. Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease this risk, regularly use a sunscreen with a Broad Spectrum SPF value of 15 or higher and other sun protection measures including: limit time in t...

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

ZINC OXIDE (22.24%)

Purpose

OTC - PURPOSE SECTION

Sunscreen

Uses

INDICATIONS & USAGE SECTION

helps prevent sunburn

if used as directed with other sun protection measures (see Directions), decreases the risk of skin cancer and early skin aging caused by the sun

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If product is swallowed, get medical help or contact a Poison Control Center right away.

Warnings

WARNINGS SECTION

For external use only

Do not use on damaged or broken skin

When using this product keep out of eyes. Rinse with water to remove.

Stop use and ask a doctor if rash occurs

Keep out of reach of children. If product is swallowed, get medical help or contact a Poison Control Center right away.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

WATER, CYCLOHEXASILOXANE, CAPRYLYL METHICONE, BUTYLENE GLYCOL, DICAPRYLATE/DICAPRATE, BUTYLOCTYL SALICYLATE, DIPROPYLENE GLYCOL, PROPYLHEPTYL CAPRYLATE, LAURYL PEG-10 TRIS(TRIMETHYLSILOXY)SILYLETHYL DIMETHICONE, METHYL METHACRYLATE CROSSPOLYMER, DISTEARDIMONIUM HECTORITE, TRIETHOXYCAPRYLYLSILANE, 1,2-HEXANEDIOL, POLYGLYCERYL-2 TRIISOSTEARATE, LAURYL POLYGLYCERYL-3 POLYDIMETHYLSILOXYETHYL DIMETHICONE, FRAGRANCE, CAPRYLYL GLYCOL, ETHYLHEXYLGLYCERIN, SODIUM HYALURONATE, TOCOPHEROL, GLYCERIN, CAPRYLIC/CAPRIC TRIGLYCERIDE, POLYGLYCERYL-10 DIISOSTEARATE, HYDROGENATED LECITHIN, MENADIONE, CENTELLA ASIATICA EXTRACT, BETA-GLUCAN

Directions

DOSAGE & ADMINISTRATION SECTION

For sunscreen use:

apply liberally 15 minutes before sun exposure
reapply at least every 2 hours
use a water-resistant sunscreen if swimming or sweating
Sun Protection Measures. Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease this risk, regularly use a sunscreen with a Broad Spectrum SPF value of 15 or higher and other sun protection measures including:

limit time in the sun, especially from 10 a.m. – 2 p.m.
wear long-resistant shirts, pants, hats, and sunglasses

children under 6 months of age: Ask a doctor

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

magnif uv defense me no sebum sun screenmagnif uv defense me no sebum sun screen

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
84523-101-022026-01-29C16284748780-149896155-a589-586f-e063-e6dba90add901c36a57a-55e6-e506-e063-6294a90acb04

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
84523-101-01UV defense me. No sebum sunscreen50 mL in 1 TUBECREAM504
84523-101-02UV defense me. No sebum sunscreen1 in 1 BOXCREAM14

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
84523-101UV DEFENSE ME. NO SEBUM SUNSCREEN (ZINC OXIDE) CREAM [MAGNIF CO., LTD]42 package rows20240720_1c36a57a-55e6-e506-e063-6294a90acb04.zip

Products#

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

DailyMed product names page 1 of 1 · 22 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
84523-10184523-101-01, 84523-101-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 21 matching rows.

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
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
1d8ec4f3-26b8-70dc-e063-6294a90a8cc81c36a57a-55e6-e506-e063-6294a90acb042024-07-18WarningsExact identifier
spl id: 1d8ec4f3-26b8-70dc-e063-6294a90a8cc8
spl set id: 1c36a57a-55e6-e506-e063-6294a90acb04

Reported adverse events (FAERS/openFDA)#

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