SUNBUM SPF 50- octisalate - 5.00% octinoxate - 7.50% oxybenzone - 6.00% zinc oxide - 7.00% cream 
Sun Bum

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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SunBum SPF 50

Active ingredients                        Purpose

Octisalate - 5.00%                          Sunscreen
Octinoxate - 7.50%
Oxybenzone - 6.00%
Zinc Oxide - 7.00%

Uses

- helps prevent sunburn
- if used as directed with other sun protection messures ( see Directions) decreases the risk of skin cancer and early skin aging caused by sun.

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 a doctor if rash occurs
Keep out of reach of children. If product is swallowed, get medical help or contact a Poison Control Center right away.

Directions

apply liberally 15 minutes before sun exposure
• reapply: • after 80 minutes of swimming or sweating
• immediately after towel drying • at least every 2 hours
Sun Protection Measures. Spending time in the sun
increases your risk of skin cancer and early skin aging.
To decrease this risk, regularly use a sunscreen with a
broad spectrum SPF of 15 or higher and other sun
protection measures including:
• limit time in the sun, especially from 10 a.m. – 2 p.m.
• wear long-sleeve shirts, pants, hats, and sunglasses
• children under 6 months: Ask a doctor

Inactive ingredients

Aloe Barbadensis Leaf Extract
Beeswax
Cetyl Dimethicone
Cetyl PEG/PPG-10/1 Dimethicone
Cyclohexasiloxane
Cyclopentasiloxane
Diisopropyl Adipate
DMDM Hydantoin
Ethylhexyl Palmitate
Ethylhexyl Stearate
Fragrance
Glycerin
Hydrated Silica
Hydrogenated Castor Oil
Polyethylene
Sodium Chloride
Theobroma Cacao (Cocoa) Seed Butter
Tocopheryl Acetate
Triethoxycaprylylsilane
Water

Package Labeling

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SUNBUM SPF 50 
octisalate - 5.00% octinoxate - 7.50% oxybenzone - 6.00% zinc oxide - 7.00% cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69039-559
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE5 g  in 100 mL
OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE7.5 g  in 100 mL
OXYBENZONE (UNII: 95OOS7VE0Y) (OXYBENZONE - UNII:95OOS7VE0Y) OXYBENZONE6 g  in 100 mL
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC CATION - UNII:13S1S8SF37) ZINC CATION7   in 100 mL
Inactive Ingredients
Ingredient NameStrength
ALOE (UNII: V5VD430YW9) 4 g  in 100 mL
YELLOW WAX (UNII: 2ZA36H0S2V)  
CETYL DIMETHICONE 45 (UNII: IK315POC44)  
CETYL PEG/PPG-10/1 DIMETHICONE (HLB 3) (UNII: G300307ZXP)  
CYCLOMETHICONE 6 (UNII: XHK3U310BA)  
CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)  
DIISOPROPYL ADIPATE (UNII: P7E6YFV72X)  
DMDM HYDANTOIN (UNII: BYR0546TOW)  
ETHYLHEXYL PALMITATE (UNII: 2865993309)  
ETHYLHEXYL STEARATE (UNII: EG3PA2K3K5)  
GLYCERIN (UNII: PDC6A3C0OX)  
HYDRATED SILICA (UNII: Y6O7T4G8P9)  
HYDROGENATED CASTOR OIL (UNII: ZF94AP8MEY)  
POLYETHYLENE GLYCOL 200 (UNII: R95B8J264J)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
COCOA BUTTER (UNII: 512OYT1CRR)  
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:69039-559-011 in 1 CARTON02/10/201108/31/2018
130 mL in 1 JAR; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart35202/10/201108/31/2018
Labeler - Sun Bum (028642574)

Revised: 2/2020
 
Sun Bum