BB SPF20- octinoxate, octisalate, oxybenzone cream 
e.l.f. Cosmetics, Inc

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BB Cream SPF20

Drug Facts

Active ingredients

Octinoxate 6%

Octisalate 4%

Oxybenzone 3.5%

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 a doctor

if rash occurs

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

Inactive ingredients

Water (Aqua), Propylene Glycol, Glycerin, C12-15 Alkyl Benzoate, Cetyl PEG/PPG-10/1 Dimethicone, Cyclopentasiloxane, Cyclohexasiloxane, Sorbitan Olivate, Polymethyl Methacrylate, Sodium Chloride, Talc, Simmondsia Chinensis (Jojoba) Seed Oil, Cucumis Sativus (Cucumber) Fruit Extract, Aloe Barbadensis Leaf Extract, Bisabolol, Tocopheryl Acetate (Ve), VP/Hexadecene Copolymer, Quaternium-18 Bentonite, Butylene Glycol, Zinc Stearate, Zinc Palmitate, Silica, Mica, Triethoxycaprylylsilane, Phenoxyethanol, Ethylhexylglycerin, Caprylyl Glycol, Fragrance (Parfum) May Contain: Titanium Dioxide (CI 77891), Iron Oxides (CI 77491, CI 77492, CI 77499)

Questions or comments?

1-855-353-7320

Package Labeling:

Outer PackageInner Package

BB SPF20 
octinoxate, octisalate, oxybenzone cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:76354-450
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE60 mg  in 1 mL
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE40 mg  in 1 mL
OXYBENZONE (UNII: 95OOS7VE0Y) (OXYBENZONE - UNII:95OOS7VE0Y) OXYBENZONE35 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
GLYCERIN (UNII: PDC6A3C0OX)  
ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)  
CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)  
CYCLOMETHICONE 6 (UNII: XHK3U310BA)  
SORBITAN OLIVATE (UNII: MDL271E3GR)  
POLY(METHYL METHACRYLATE; 450000 MW) (UNII: Z47NNT4J11)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
TALC (UNII: 7SEV7J4R1U)  
JOJOBA OIL (UNII: 724GKU717M)  
CUCUMBER (UNII: YY7C30VXJT)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
LEVOMENOL (UNII: 24WE03BX2T)  
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
VINYLPYRROLIDONE/HEXADECENE COPOLYMER (UNII: KFR5QEN0N9)  
BENTOQUATAM (UNII: 7F465U79Q1)  
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
ZINC STEARATE (UNII: H92E6QA4FV)  
ZINC PALMITATE (UNII: Q7407964JA)  
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
MICA (UNII: V8A1AW0880)  
TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:76354-450-281 in 1 BOX10/20/2019
128.5 mL in 1 BOTTLE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM02010/20/2019
Labeler - e.l.f. Cosmetics, Inc (093902816)

Revised: 11/2023
Document Id: 09886422-4451-1e78-e063-6394a90a07a8
Set id: 25b6dc60-7480-42cf-acd3-4155d6e57b1f
Version: 5
Effective Time: 20231106
 
e.l.f. Cosmetics, Inc