EXTREME PROTECT SPF 30- octinoxate, zinc oxide lotion 
SCIENCE OF SKINCARE LLC

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Extreme Protect SPF 30

Active Ingredients

Octinoxate – 5.50%

Zinc Oxide – 4.12%

PURPOSE

SUNSCREEN

USES

• Helps prevent sunburn.
• If used as directed with other sun protection measures (see Directions), decreases the risk of skin cancer and early skin aging caused by the 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

DIRECTIONS

• Use a water resistant sunscreen if swimming or sweating

• Reapply 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:
o limit time in the sun, especially from 10 a.m.-2 p.m.
o wear long-sleeve shirts, pants, hats, and sunglasses
• Children under 6 months: Ask a doctor

Other Information

PROTECT THIS PRODUCT FROM EXCESSIVE HEAT AND DIRECT SUN.

Questions or Comments?

Call Customer Care at (888) 804-4447

Inactive Ingredients

Water, Polyacrylamide, Tocopherol, Ethylhexyl Palmitate, PPG-3 Myristyl Ether, Cetyl Alcohol, Glycol Stearate SE, VP/Hexadecene Copolymer, Olea Europaea (Olive) Leaf Extract, Aloe Barbadensis Leaf Juice, Asiaticoside, Asiatic Acd, Madecassic Acid, Sodium Dihydrocetyl Phosphate, Ethyl Linoleate, Oleyl Alcohol, Glyceryl Stearate, Octyldodecyl Neopentanoate, Caprylyl Glycol, Hexylene Glycol, PEG-100 Stearate, C13-14 Isoparaffin, Laureth-7, Phenoxyethanol.

Package Label - Principal Display Panel

100g Label NDC 69219-103-13100g Box NDC 69219-103-51240g Box NDC 69219-103-585g Pack NDC 69219-103-55240g Label NDC 69219-103-285g Label NDC 69219-103-15

EXTREME PROTECT SPF 30 
octinoxate, zinc oxide lotion
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69219-103
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE5.5 g  in 100 g
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC CATION - UNII:13S1S8SF37) ZINC CATION4.12 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
POLYACRYLAMIDE (1500 MW) (UNII: 5D6TC4BRWV)  
TOCOPHEROL (UNII: R0ZB2556P8)  
ETHYLHEXYL PALMITATE (UNII: 2865993309)  
PPG-3 MYRISTYL ETHER (UNII: 7913J43WZ5)  
CETYL ALCOHOL (UNII: 936JST6JCN)  
GLYCOL STEARATE SE (UNII: 6YLY96TQL6)  
VINYLPYRROLIDONE/HEXADECENE COPOLYMER (UNII: KFR5QEN0N9)  
OLEA EUROPAEA LEAF (UNII: MJ95C3OH47)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
ASIATICOSIDE (UNII: PKO39VY215)  
ASIATIC ACID (UNII: 9PA5A687X5)  
MADECASSIC ACID (UNII: M7O1N24J82)  
SODIUM DIHYDROXYCETYL PHOSPHATE (UNII: YWI33EV595)  
ETHYL LINOLEATE (UNII: MJ2YTT4J8M)  
OLEYL ALCOHOL (UNII: 172F2WN8DV)  
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  
OCTYLDODECYL NEOPENTANOATE (UNII: X8725R883T)  
CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
HEXYLENE GLYCOL (UNII: KEH0A3F75J)  
PEG-100 STEARATE (UNII: YD01N1999R)  
C13-14 ISOPARAFFIN (UNII: E4F12ROE70)  
LAURETH-7 (UNII: Z95S6G8201)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:69219-103-511 in 1 BOX10/01/2014
1NDC:69219-103-13100 g in 1 BOTTLE, PUMP; Type 0: Not a Combination Product
2NDC:69219-103-551 in 1 BOX10/01/2014
2NDC:69219-103-155 g in 1 BOTTLE, PUMP; Type 0: Not a Combination Product
3NDC:69219-103-28240 g in 1 BOTTLE, PUMP; Type 0: Not a Combination Product10/01/2014
4NDC:69219-103-13100 g in 1 BOTTLE, PUMP; Type 0: Not a Combination Product10/01/2014
5NDC:69219-103-155 g in 1 BOTTLE, PUMP; Type 0: Not a Combination Product10/01/2014
6NDC:69219-103-581 in 1 BOX08/01/2023
6240 g in 1 BOTTLE, PUMP; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM02010/01/2014
Labeler - SCIENCE OF SKINCARE LLC (006251958)

Revised: 12/2023
Document Id: 0c7f5769-e88b-acc1-e063-6294a90afc7e
Set id: ecc4d304-e7e2-45b6-b9b2-2c64d3630860
Version: 9
Effective Time: 20231214
 
SCIENCE OF SKINCARE LLC