SUNNYLIFE SPF 50+ SUNSCREEN FRAGRANCE FREE LOTION JNR

Manufacturer: OUTLIVING PTY LTD | Baxter Laboratories Pty. Ltd.
Effective date: 2018-11-08
Label type: HUMAN OTC DRUG LABEL
Version: 2
Source: full-release
Hydrated at: 2026-05-31 22:58:05

Label at a glance#

ProductSUNNYLIFE SPF 50 SUNSCREEN FRAGRANCE FREE

Active ingredientAVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE

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 & early skin aging caused by the sun.

Contacts and useful links#

PhoneLabel contact+1 323.591.0219

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS:

OTC - ACTIVE INGREDIENT SECTION

Avobenzone 3%, Homosalate 10%

Ocitsalate 5% Octocrylene 8%

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 & early skin aging caused by the sun.

WARNINGS:

WARNINGS SECTION

For external use only.

Do not use

OTC - DO NOT USE SECTION

on damaged or broken skin.

When using this product

OTC - WHEN USING SECTION

keep out of eyes. Rinse with water to remove.

Stop use and ask doctor

OTC - STOP USE SECTION

if rash occurs.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If product is swallowed, get medical help contact Poison Control Center right away.

DIRECTION:

DOSAGE & ADMINISTRATION SECTION

For sunscreen use
Apply generously 15 minutes before sun exposure. Reapply:
After 80 minutes of swimming or sweating
Immediately after towel drying
At least every 2 hours. Skin Protection Measures. Spending time in the sun increases your risk of skin cancer & early sking aging. To decrease this risk, regularly use a sunscreen with broad spectrum SPF of 15 or higher & other sun protection measures including:
Limit time in the sun, especially from 10am-2pm
Wear long-sleeve shirts, pants, hats and sunglasses.
Children under 6 months: ask a doctor.

OTHER INFORMATION:

SPL UNCLASSIFIED SECTION

Protect this product from excessive heat and direct sun.

INACTIVE INGREDIENTS:

INACTIVE INGREDIENT SECTION

Water, Cera Alba, C12-15 Alkyl Benzoate, SIlica, PEG-15 Cocamine, PEG-40 Stearate, Carbomer, Hydroxyethylcellulose, Caprylhydroxamic Acid, Caprylyl Glycol, Glycerin, Triethanolamine, Aloe Barbadensis Leaf Juice, Tocopheryl Acetate, Citric Acid.

QUESTIONS OR COMMENTS?

OTC - QUESTIONS SECTION

+1 323.591.0219

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
72566-050-06	2020-01-31	C162847	48780-1	9d75b9d0-3859-f424-e053-dadaa90a57ce	SUNNYLIFE SPF 50+ SUNSCREEN FRAGRANCE FREE LOTION JNR

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
72566-050-06	SUNNYLIFE SPF 50 SUNSCREEN FRAGRANCE FREE	200 mL in 1 BOTTLE	LOTION	200		2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
72566-050	SUNNYLIFE SPF 50 SUNSCREEN FRAGRANCE FREE (AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE) LOTION [OUTLIVING PTY LTD]	2	Legacy NDC, 1 package rows	20190106_18fae8fb-de2d-469c-a83d-f5ec76f6ea94.zip

Products#

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

DailyMed product names page 1 of 1 · 19 matching rows.

SUNNYLIFE SPF 50 SUNSCREEN FRAGRANCE FREE
AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE
WATER
WHITE WAX
ALKYL (C12-15) BENZOATE
SILICON DIOXIDE
PEG-15 COCAMINE
PEG-40 STEARATE
CARBOXYPOLYMETHYLENE
CAPRYLHYDROXAMIC ACID
CAPRYLYL GLYCOL
GLYCERIN
TROLAMINE
ALOE VERA LEAF
CITRIC ACID MONOHYDRATE
AVOBENZONE
HOMOSALATE
OCTISALATE
OCTOCRYLENE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
72566-050	72566-050-06

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 17 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
WATER	059QF0KO0R	IACT
WHITE WAX	7G1J5DA97F	IACT
ALKYL (C12-15) BENZOATE	A9EJ3J61HQ	IACT
SILICON DIOXIDE	ETJ7Z6XBU4	IACT
PEG-15 COCAMINE	8L6LB12TSJ	IACT
PEG-40 STEARATE	ECU18C66Q7	IACT
CARBOXYPOLYMETHYLENE	0A5MM307FC	IACT
CAPRYLHYDROXAMIC ACID	UPY805K99W	IACT
CAPRYLYL GLYCOL	00YIU5438U	IACT
GLYCERIN	PDC6A3C0OX	IACT
TROLAMINE	9O3K93S3TK	IACT
ALOE VERA LEAF	ZY81Z83H0X	IACT
CITRIC ACID MONOHYDRATE	2968PHW8QP	IACT
AVOBENZONE	G63QQF2NOX	ACTIB
HOMOSALATE	V06SV4M95S	ACTIB
OCTISALATE	4X49Y0596W	ACTIB
OCTOCRYLENE	5A68WGF6WM	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
7a253740-4a27-8e8f-e053-2991aa0a7282			18fae8fb-de2d-469c-a83d-f5ec76f6ea94	2018-11-08	Warnings	Exact identifier spl id: 7a253740-4a27-8e8f-e053-2991aa0a7282 spl set id: 18fae8fb-de2d-469c-a83d-f5ec76f6ea94

Reported adverse events (FAERS/openFDA)#

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