BOBBI BROWN SKIN FOUNDATION BROAD SPECTRUM SPF 15- octinoxate and titanium dioxide liquid 
Bobbi Brown Professional Cosmetics Inc.

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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BOBBI BROWN SKIN FOUNDATION

BROAD SPECTRUM SPF 15

Drug Facts

Active Ingredients

Octinoxate 7.50%
Titanium Dioxide 1.00%

Purpose

Sunscreen

Use

Helps prevent sunburn

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

For sunscreen use:

Inactive ingredients

water\aqua\eau • methyl trimethicone • neopentyl glycol diethylhexanoate • isononyl isononanoate • glycerin • pentylene glycol • lauryl peg-9 polydimethylsiloxyethyl dimethicone • hdi/trimethylol hexyllactone crosspolymer • talc • boron nitride • disteardimonium hectorite • stearic acid • palmitic acid • dimethicone • lecithin • aluminum dimyristate • tocopherol • myristic acid • silica • magnesium ascorbyl phosphate • sodium chloride • sodium citrate • sorbic acid • chlorphenesin • phenoxyethanol • [+/- titanium dioxide (ci 77891) • iron oxides (ci 77491, ci 77492, ci 77499)] <iln34969>

Other information

Protect the product in this container from excessive heat and direct sun.

Dist. Bobbi Brown Professional Cosmetics
N.Y., N.Y. 10022

PRINCIPAL DISPLAY PANEL - 30 mL Bottle Carton

BOBBI
BROWN

Skin Foundation
Broad Spectrum SPF 15

1 FL. OZ./ 30 ml e

Principal Display Panel - 30 mL Bottle Carton
BOBBI BROWN SKIN FOUNDATION  BROAD SPECTRUM SPF 15
octinoxate and titanium dioxide liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:64141-013
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE75 mg  in 1 mL
TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) TITANIUM DIOXIDE10 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
METHYL TRIMETHICONE (UNII: S73ZQI0GXM)  
NEOPENTYL GLYCOL DIETHYLHEXANOATE (UNII: U68ZV6W62C)  
ISONONYL ISONONANOATE (UNII: S4V5BS6GCX)  
GLYCERIN (UNII: PDC6A3C0OX)  
PENTYLENE GLYCOL (UNII: 50C1307PZG)  
TALC (UNII: 7SEV7J4R1U)  
BORON NITRIDE (UNII: 2U4T60A6YD)  
STEARIC ACID (UNII: 4ELV7Z65AP)  
PALMITIC ACID (UNII: 2V16EO95H1)  
DIMETHICONE (UNII: 92RU3N3Y1O)  
ALUMINUM DIMYRISTATE (UNII: J2KA067N9O)  
TOCOPHEROL (UNII: R0ZB2556P8)  
MYRISTIC ACID (UNII: 0I3V7S25AW)  
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
MAGNESIUM ASCORBYL PHOSPHATE (UNII: 0R822556M5)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM CITRATE, UNSPECIFIED FORM (UNII: 1Q73Q2JULR)  
SORBIC ACID (UNII: X045WJ989B)  
CHLORPHENESIN (UNII: I670DAL4SZ)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
FERRIC OXIDE RED (UNII: 1K09F3G675)  
FERRIC OXIDE YELLOW (UNII: EX438O2MRT)  
FERROSOFERRIC OXIDE (UNII: XM0M87F357)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:64141-013-011 in 1 CARTON09/01/2012
130 mL in 1 BOTTLE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalM02009/01/2012
Labeler - Bobbi Brown Professional Cosmetics Inc. (627131279)
Registrant - Estee Lauder Companies Inc. (790802086)
Establishment
NameAddressID/FEIBusiness Operations
JO COSMETICS691485222manufacture(64141-013)

Revised: 7/2023
Document Id: 017abe9e-16e6-538e-e063-6294a90accc2
Set id: a3329e11-8f1b-4e66-8b51-4ba0208612fd
Version: 10
Effective Time: 20230727
 
Bobbi Brown Professional Cosmetics Inc.