SUN Solar Defense Oil-free Gel SPF 15

Manufacturer: Allure Labs, Inc.
Effective date: 2010-07-01
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 22:24:59

Label at a glance#

ProductSUN Solar Defense Oil-free Gel SPF 15

Active ingredientTITANIUM DIOXIDE, OCTINOXATE, OXYBENZONE

Label structure6 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredients:

Titanium Dioxide 1.6%

Ethylhexyl Methoxycinnamate (Octinoxate) 7.50%

Benzophenone-3: 3.00%

OTC - PURPOSE SECTION

Purpose:

Sunscreen

INDICATIONS & USAGE SECTION

Uses:

An oil-free UVA/UVB broad spectrum daily moisturizer. Provides ultimate protection against the aging effects of the sun and other environmental exposure. Enriched with essential vitamins and anti-oxidants that prevent free radical damage and preserving skin hydration for the entire day.
Water-resistant
Paraben-free

Directions:

Apply liberally 15-30 minute prior to sun exposure. Reapply after prolonged swimming or vigorous activity.

Indications:

Universal for all skin types.

WARNINGS SECTION

Warnings:

For external use only.

When using this product

Keep out of eyes. If contact occurs rinse with water.
Discontinue use if irritation or redness occurs.

Keep out of reach of children

INACTIVE INGREDIENT SECTION

Inactive Ingredients:

Water (Aqua), Ethylhexyl Methoxycinnamate, Ascorbyl Palmitate, Cyclomethicone, Benzophenone-3, Glycerin, Glyceryl Stearate, Camellia Sinensis Leaf Extract (Green Tea), Tocopheryl Acetate, Phenoxyethanol, Lecithin, C13-14 Isoparaffin Citrus blend, Xanthan Gum, Disodium EDTA.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Distributor:

Image International
Palm Beach, FL 33411 USA

Image of the product:

Sun Solar Defense Oil-free Gel SPF 15

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
62742-4039-1	2019-10-21	C162847	48780-1	956f9ecf-c600-621f-e053-dbdaa90a74ad	Drug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
62742-4039-1	SUN Solar Defense Oil-free Gel SPF 15	118 mL in 1 TUBE	CREAM	118		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
62742-4039	SUN SOLAR DEFENSE OIL-FREE GEL SPF 15 (TITANIUM DIOXIDE, ETHYLHEXYL METHOXYCINNAMATE, BENZOPHENONE-3) CREAM [ALLURE LABS, INC.]	1	Legacy NDC, 1 package rows	20100702_197a68f8-ba73-432f-b215-f715a494d06d.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	SPL version
OCTINOXATE	ACTIVE INGREDIENT	4Y5P7MUD51	1
OXYBENZONE	ACTIVE INGREDIENT	95OOS7VE0Y	1
TITANIUM DIOXIDE	ACTIVE INGREDIENT	15FIX9V2JP	1
OCTINOXATE	ACTIVE MOIETY	4Y5P7MUD51	1
OXYBENZONE	ACTIVE MOIETY	95OOS7VE0Y	1
TITANIUM DIOXIDE	ACTIVE MOIETY	15FIX9V2JP	1

Products#

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

DailyMed product names page 1 of 1 · 5 matching rows.

SUN Solar Defense Oil-free Gel SPF 15
Titanium Dioxide, Ethylhexyl Methoxycinnamate, Benzophenone-3
TITANIUM DIOXIDE
OCTINOXATE
OXYBENZONE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
62742-4039	62742-4039-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
TITANIUM DIOXIDE	15FIX9V2JP	ACTIB
OCTINOXATE	4Y5P7MUD51	ACTIB
OXYBENZONE	95OOS7VE0Y	ACTIB

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
1f4eca23-2fe7-4ba0-8e19-7923e510efa8			197a68f8-ba73-432f-b215-f715a494d06d	2010-07-01	Warnings	Exact identifier spl id: 1f4eca23-2fe7-4ba0-8e19-7923e510efa8 spl set id: 197a68f8-ba73-432f-b215-f715a494d06d

Reported adverse events (FAERS/openFDA)#

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