SUNNYLIFE SPF 50+ SUNSCREEN COCONUT SCENTED LOTION

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 COCONUT SCENTED
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.

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, Fragrance, 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

Label2Label2

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
3c386306-c48a-413e-bb69-70cb268496f3Product name120210727

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
72566-051-062020-01-31C16284748780-19d75b9d0-3856-f424-e053-dadaa90a57ceSUNNYLIFE SPF 50+ SUNSCREEN COCONUT SCENTED LOTION

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72566-051-06SUNNYLIFE SPF 50 SUNSCREEN COCONUT SCENTED200 mL in 1 BOTTLELOTION2002

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
72566-051SUNNYLIFE SPF 50 SUNSCREEN COCONUT SCENTED (AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE) LOTION [OUTLIVING PTY LTD]2Legacy NDC, 1 package rows20190106_01fd3dc4-b804-424f-94ed-a73c73e0207b.zip

Products#

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

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

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72566-05172566-051-06

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 17 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
7a258134-40cc-39bf-e053-2a91aa0a1aac01fd3dc4-b804-424f-94ed-a73c73e0207b2018-11-08WarningsExact identifier
spl id: 7a258134-40cc-39bf-e053-2a91aa0a1aac
spl set id: 01fd3dc4-b804-424f-94ed-a73c73e0207b

Reported adverse events (FAERS/openFDA)#

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