CLINIQUE BROAD SPECTRUM SPF 30 SUNSCREEN FACE CREAM WITH SOLAR SMART

Manufacturer
CLINIQUE LABORATORIES LLC | 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
2019-11-20
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 23:58:02

Label at a glance#

ProductCLINIQUE BROAD SPECTRUM SPF 30 SUNSCREEN FACE WITH SOLAR SMART
Active ingredientAVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE, OXYBENZONE
Label structure9 sections

Dosage and administration

For sunscreen use: apply liberally 15 minutes before sun exposure reapply at least every two hours use a water resistant sunscreen if swimming or sweating 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...

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 3.0%
Homosalate 5.0%
Octisalate 5.0%
Octocrylene 2.7%
Oxybenzone 4.0%

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:

  • apply liberally 15 minutes before sun exposure
  • reapply at least every two hours
  • use a water resistant sunscreen if swimming or sweating
  • 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

water\aqua\eau • methyl trimethicone • butylene glycol • butyloctyl salicylate • neopentyl glycol diheptanoate • butyrospermum parkii (shea butter) • peg-100 stearate • silica • dipentaerythrityl tri-polyhydroxystearate • lauryl peg-9 polydimethylsiloxyethyl dimethicone • dimethicone • glyceryl stearate • laurdimonium hydroxypropyl hydrolyzed soy protein • rosmarinus officinalis (rosemary) extract • perilla ocymoides leaf extract • plankton extract • caffeine • potassium cetyl phosphate • sucrose • styrene/acrylates copolymer • c30-38 olefin/isopropyl maleate/ma copolymer • cetyl alcohol • vp/eicosene copolymer • ethylhexylglycerin • ammonium acryloyldimethyltaurate/vp copolymer • peg-8 laurate • sodium rna • lecithin • propyl gallate • arginine ferulate • tocopheryl acetate • caprylyl glycol • ascorbyl tocopheryl maleate • stearic acid • xanthan gum • hexylene glycol • nordihydroguaiaretic acid • disodium edta • phenoxyethanol • mica • sodium dehydroacetate [iln37116]

Other information

STORAGE AND HANDLING SECTION

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

PRINCIPAL DISPLAY PANEL - 50 ml Tube Carton

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

CLINIQUE

broad
spectrum
SPF 30
sunscreen

with
SolarSmart

UVA UVB
PROTECTION

face cream

1.7 FL. OZ.
50 ml e

PRINCIPAL DISPLAY PANEL - 50 ml Tube Carton
PRINCIPAL DISPLAY PANEL - 50 ml Tube Carton

Products#

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
49527-06449527-064-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 38 matching rows.

Source Document#

Source XML · Source PDF

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
c345ca32-5451-4bc0-a9db-cc567adad16bbf6d9bae-1986-4430-b2bc-8ce6d0b6a7102020-11-16WarningsExact identifier
spl set id: bf6d9bae-1986-4430-b2bc-8ce6d0b6a710

Reported adverse events (FAERS/openFDA)#

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