SPF 50 SIGNATURE HIGH PERFORMANCE SUNSCREEN- octinoxate, octisalate, octocrylene, zinc oxide lotion

SPF 50 Signature High Performance Sunscreen by

Drug Labeling and Warnings

SPF 50 Signature High Performance Sunscreen by is a Otc medication manufactured, distributed, or labeled by Sun Bum LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active Ingredients

Octinoxate 7.5%, Octisalate 5%, Octocrylene 7%, Zinc oxide 10%

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.

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.
• Children under 6 months: Ask a doctor.
• 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 Broad Spectrum SPF of 15 or higher and other sun protection measures, including:
• Limit time in the sun, especially from 10 am - 2 pm.
• Wear long-sleeved shirts, pants, hats, and sunglasses.

Inactive Ingredients

water, C12-15 alkyl benzoate, trimethylpentanediol/adipic acid copolymer, arachidyl alcohol, butyrospermum parkii (shea) butter, glycerin, polyester-8, aloe barbadensis leaf juice, tocopheryl acetate, sorbitol, beeswax, xanthan gum, lecithin, oleic Acid, caprylyl glycol, disodium EDTA, glyceryl caprylate, phenoxyethanol, sorbitan oleate, hydroxyethyl acrylate/sodium acryloyldimethyl taurate, panthenol, ethylhexylglycerin, sodium hyaluronate, ascorbyl palmitate, behenyl alcohol, arachidyl glucoside, methylisothiazolinone, CI 77491

Other Information

• Protect this product from excessive heat and directed sun.

Questions?

Call 1-877-978-6286

Package Labeling:

INGREDIENTS AND APPEARANCE

SPF 50 SIGNATURE HIGH PERFORMANCE SUNSCREEN 
octinoxate, octisalate, octocrylene, zinc oxide lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69039-228
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51)	OCTINOXATE	75 mg  in 1 mL
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W)	OCTISALATE	50 mg  in 1 mL
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM)	OCTOCRYLENE	70 mg  in 1 mL
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC CATION - UNII:13S1S8SF37)	ZINC CATION	100 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
ARACHIDYL ALCOHOL (UNII: 1QR1QRA9BU)
SHEA BUTTER (UNII: K49155WL9Y)
GLYCERIN (UNII: PDC6A3C0OX)
POLYESTER-8 (1400 MW, CYANODIPHENYLPROPENOYL CAPPED) (UNII: T9296U138P)
SORBITOL (UNII: 506T60A25R)
YELLOW WAX (UNII: 2ZA36H0S2V)
XANTHAN GUM (UNII: TTV12P4NEE)
OLEIC ACID (UNII: 2UMI9U37CP)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)
GLYCERYL MONOCAPRYLATE (UNII: TM2TZD4G4A)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
SORBITAN MONOOLEATE (UNII: 06XEA2VD56)
HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER (100000 MPA.S AT 1.5%) (UNII: 86FQE96TZ4)
PANTHENOL (UNII: WV9CM0O67Z)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
HYALURONATE SODIUM (UNII: YSE9PPT4TH)
ASCORBYL PALMITATE (UNII: QN83US2B0N)
DOCOSANOL (UNII: 9G1OE216XY)
ARACHIDYL GLUCOSIDE (UNII: 6JVW35JOOJ)
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
FERRIC OXIDE RED (UNII: 1K09F3G675)

Product Characteristics
Color	white	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 69039-228-01	947 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/03/2012

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part352	05/03/2012

Labeler - Sun Bum LLC (028642574)