FDA.reportPublic FDA data

BOBBI BROWN BEACH SUNSCREEN BODY SPRAY BROAD SPECTRUM SPF 15

Manufacturer
Bobbi Brown Professional Cosmetics Inc. | ESTEE LAUDER COMPANY, THE | ESTEE LAUDER COSMETICS, LTD | ESTEE LAUDER COSMETICS, LTD. | ESTEE LAUDER N.V. | LEN-RON MANUFACTURING DIVISION OF ARAMIS INC | NORTHTEC INC | PADC 1 | WHITMAN LABORATORIES, LTD.
Effective date
2018-11-27
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-02 00:45:25

Label at a glance#

ProductBOBBI BROWN BEACH SUNSCREEN BODY BROAD SPECTRUM SPF 15
Active ingredientAVOBENZONE, OCTINOXATE, OCTISALATE, OCTOCRYLENE
Label structure9 sections

Dosage and administration

For sunscreen use: spray generously and spread evenly by hand 15 minutes before sun exposure reapply at least every two hours and immediately after towel drying, and after 40 minutes of swimming or perspiring 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 value of 15 or higher and ...

Storage and handling

protect the product in this container from excessive heat and direct sun

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Avobenzone 2.0%
Octinoxate 5.0%
Octisalate 4.5%
Octocrylene 2.8%

Purpose

OTC - PURPOSE SECTION

Sunscreen

Use

INDICATIONS & USAGE SECTION

helps prevent sunburn

Warnings

WARNINGS SECTION

For external use only

OTC - DO NOT USE SECTION

Do not use on damaged or broken skin

OTC - WHEN USING SECTION

When using this product keep out of eyes. Rinse with water to remove.

OTC - STOP USE SECTION

Stop use and ask a doctor if rash occurs.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

For sunscreen use:

  • spray generously and spread evenly by hand 15 minutes before sun exposure
  • reapply at least every two hours and immediately after towel drying, and after 40 minutes of swimming or perspiring
  • 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 value 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-sleeved shirts, pants, hats and sunglasses
  • children under 6 months of age: ask a doctor

Inactive ingredients

INACTIVE INGREDIENT SECTION

olea europaea (olive) fruit oil • octyldodecyl neopentanoate • vitis vinifera (grape) seed oil • caprylic/capric triglyceride • pvp/hexadecene copolymer • ricinus communis (castor) seed oil • fragrance (parfum) • cholesterol • linoleic acid • tocopheryl acetate • bht • hydroxycitronellal • geraniol • benzyl salicylate • hexyl cinnamal • amyl cinnamal • linalool • limonene • citronellol • benzyl benzoate • cinnamyl alcohol • farnesol • citral • phenoxyethanol <iln43472>

Other information

STORAGE AND HANDLING SECTION

protect the product in this container from excessive heat and direct sun

PRINCIPAL DISPLAY PANEL - 200 ml Bottle Carton

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

BOBBI BROWN
Beach

Sunscreen Body Spray
Broad Spectrum SPF 15

6.7 FL. OZ. LIQ./200 ml e

PRINCIPAL DISPLAY PANEL - 200 ml Bottle Carton
PRINCIPAL DISPLAY PANEL - 200 ml Bottle Carton

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
64141-024-012021-08-09C16284748780-1c7ccaba7-15fc-fd44-e053-dadaa90aa01bBOBBI BROWN BEACH SUNSCREEN BODY SPRAY BROAD SPECTRUM SPF 15
64141-024-012021-07-23C16284748780-1c7ccaba7-15fc-fd44-e053-dadaa90aa01bBOBBI BROWN BEACH SUNSCREEN BODY SPRAY BROAD SPECTRUM SPF 15

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 28 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
64141-02464141-024-01

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 26 matching rows.

Name, UNII, Kind table
NameUNIIKind
AVOBENZONEG63QQF2NOXACTIB
OCTINOXATE4Y5P7MUD51ACTIB
OCTISALATE4X49Y0596WACTIB
OCTOCRYLENE5A68WGF6WMACTIB
OLIVE OIL6UYK2W1W1EIACT
OCTYLDODECYL NEOPENTANOATEX8725R883TIACT
GRAPE SEED OIL930MLC8XGGIACT
MEDIUM-CHAIN TRIGLYCERIDESC9H2L21V7UIACT
CASTOR OILD5340Y2I9GIACT
CHOLESTEROL97C5T2UQ7JIACT
LINOLEIC ACID9KJL21T0QJIACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
BUTYLATED HYDROXYTOLUENE1P9D0Z171KIACT
HYDROXYCITRONELLAL8SQ0VA4YURIACT
GERANIOLL837108USYIACT
BENZYL SALICYLATEWAO5MNK9TUIACT
.ALPHA.-HEXYLCINNAMALDEHYDE7X6O37OK2IIACT
.ALPHA.-AMYLCINNAMALDEHYDEWC51CA3418IACT
LINALOOL, (+/-)-D81QY6I88EIACT
LIMONENE, (+)-GFD7C86Q1WIACT
.BETA.-CITRONELLOL, (R)-P01OUT964KIACT
BENZYL BENZOATEN863NB338GIACT
CINNAMYL ALCOHOLSS8YOP444FIACT
FARNESOLEB41QIU6JLIACT
CITRALT7EU0O9VPPIACT
PHENOXYETHANOLHIE492ZZ3TIACT

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
f71e413a-8be4-491a-a433-8b32389dc7ddde92bf25-9714-4b8a-9aca-74fe94d0ac892021-08-09WarningsExact identifier
spl set id: de92bf25-9714-4b8a-9aca-74fe94d0ac89

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.