SUNNYLIFE SPF 50 SUNSCREEN FRAGRANCE FREE- avobenzone, homosalate, octisalate, octocrylene lotion 
OUTLIVING PTY LTD

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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SUNNYLIFE SPF 50+ SUNSCREEN FRAGRANCE FREE LOTION JNR

DRUG FACTS

ACTIVE INGREDIENTS:

Avobenzone 3%, Homosalate 10%

Ocitsalate 5% Octocrylene 8%

PURPOSE

Sunscreen

Uses:

WARNINGS:

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 doctor 

   if rash occurs.

Keep out of reach of children.

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

DIRECTION:

OTHER INFORMATION:

Protect this product from excessive heat and direct sun.

INACTIVE INGREDIENTS:

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?

+1 323.591.0219

Package Labeling:

Label

SUNNYLIFE SPF 50 SUNSCREEN FRAGRANCE FREE 
avobenzone, homosalate, octisalate, octocrylene lotion
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:72566-050
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE30 mg  in 1 mL
HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE100 mg  in 1 mL
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE50 mg  in 1 mL
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE80 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
WHITE WAX (UNII: 7G1J5DA97F)  
ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)  
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
PEG-15 COCAMINE (UNII: 8L6LB12TSJ)  
PEG-40 STEARATE (UNII: ECU18C66Q7)  
CARBOXYPOLYMETHYLENE (UNII: 0A5MM307FC)  
CAPRYLHYDROXAMIC ACID (UNII: UPY805K99W)  
CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
GLYCERIN (UNII: PDC6A3C0OX)  
TROLAMINE (UNII: 9O3K93S3TK)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:72566-050-06200 mL in 1 BOTTLE; Type 0: Not a Combination Product01/06/2019
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart35201/06/2019
Labeler - OUTLIVING PTY LTD (745474788)
Establishment
NameAddressID/FEIBusiness Operations
Baxter Laboratories Pty. Ltd.740537709manufacture(72566-050)

Revised: 11/2018
Document Id: 7a253740-4a27-8e8f-e053-2991aa0a7282
Set id: 18fae8fb-de2d-469c-a83d-f5ec76f6ea94
Version: 2
Effective Time: 20181108
 
OUTLIVING PTY LTD