Dr LeE UV ICE SHIELD

Manufacturer
DRLEECOSMETIC | Seoul cosmetics co.,ltd
Effective date
2017-04-11
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:49:33

Label at a glance#

ProductDr LeE UV ICE SHIELD
Active ingredientTitanium Dioxide, Octinoxate, Zinc Oxide, Octisalate
Label structure6 sections

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

Active ingredients: Titanium Dioxide 2.85%, Ethylhexyl Methoxycinnamate 2.14%, Zinc Oxide 1.61%, Ethylhexyl Salicylate 1.43%

INACTIVE INGREDIENT

INACTIVE INGREDIENT SECTION

Inactive ingredients: Butane, Propane, Water, Cyclopentasiloxane, Alcohol Denat., Propanediol, C13-15 Alkane, Bis-Ethylhexyloxyphenol methoxyphenyl triazine, Niacinamide, Talc, 1,2-Hexanedio, Lauryl PEG-8 Dimethicone, Centella Asiatica Leaf Extract, Portulaca Oleracea Extract, Melaleuca Alternifolia (Tea Tree) Extract, Nymphaea Alba Flower Extract, LavandulaAngustifolia (Lavender) Extract, CI 77492, Polyglyceryl-6 Polyricinoleate, Hydrogen Dimethicone, Polymethyl Methacrylate, CI 77491, Lauryl PEG-9 polydimethylsiloxyethyl dimethicone, Aluminium Hydroxide, Stearic Acid, Ultramarines, CI 77499, Butylene Glycol, Adenosine, Triethoxycaprylylsilane, Triethoxylsilylethyl PolydimethylsiloxyethylHexyl Dimethicone, Caprylyl Glycol, Disodium EDTA, Parfum

PURPOSE

OTC - PURPOSE SECTION

Purpose: Sunscreen

WARNINGS

WARNINGS SECTION

Warnings:

For external use only Do not use on damaged broken skin Do not store at any high or low temperature or sunlight. Product uses high pressure gas flammable. Shake well before use Do not spray over 3 second on same place, face, must use on hand and then spread it on face If possible spray the product from 20cm or farther from body Do not inhale spray gas When using this product

Avoid contact with eyes. Discontinue use if signs of irritation or rashes appear. Replace the cap after use. Before dispose gas must be removed. Do not use near fire, heating device such as heater

Keep Out of Reach of Children

DESCRIPTION

DESCRIPTION SECTION

Uses: Helps prevent sunburn

Directions 1. Turn the top of the container to “ON” 2. Shake the container up and down before use 3. And then pump 4-5 times 4. Open the cap and lightly apply on skin with the puff in a tapping motion (If the puff is too cold, wait for 5 seconds, and then evenly spread in a stroking motion) 5. After use, put the puff back in the container, close the cap and then turn the top of the container to “OFF” (Do not spray when closed)

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of cartonImage of carton

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
ZINC CATION Pharmacologic Class Indexing2Indexing - Pharmacologic Class20180813

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
f47a510b-6679-4664-b2d6-47b5c4afe7ccProduct name420260217
030ce964-9b2d-45aa-b5d3-f78ce03ef61cProduct name220250515
0306390c-dd77-4363-afe0-63c58088b2a1Product name120220120
503ea967-4b9c-48cf-9e87-c7975295849dProduct name220220120
190f2a5b-bbc8-65c7-fcb0-97891307b917Product name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
71367-010-022020-01-31C16284748780-19d75b9cf-ff2f-f424-e053-dadaa90a57ce61da0382-e6a8-4d1f-b6fa-1245eb211e3a

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
71367-010-01Dr LeE UV ICE SHIELD100 mL in 1 BOTTLECREAM1001
71367-010-02Dr LeE UV ICE SHIELD1 in 1 CARTONCREAM11

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71367-010DR LEE UV ICE SHIELD (TITANIUM DIOXIDE, OCTINOXATE, ZINC OXIDE, OCTISALATE) CREAM [DRLEECOSMETIC]1Legacy NDC, 2 package rows20170411_61da0382-e6a8-4d1f-b6fa-1245eb211e3a.zip

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
71367-01071367-010-01, 71367-010-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 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
6725b42b-e620-442f-b2cc-a1dd6e4b2eb661da0382-e6a8-4d1f-b6fa-1245eb211e3a2017-04-11WarningsExact identifier
spl id: 6725b42b-e620-442f-b2cc-a1dd6e4b2eb6
spl set id: 61da0382-e6a8-4d1f-b6fa-1245eb211e3a

Reported adverse events (FAERS/openFDA)#

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