L'BEL Défense Total Compact Cream Suncreen SPF 50 For Face - Matte Finish

Manufacturer
Ventura Corporation LTD | Bel Star S.A. (Colombia)
Effective date
2017-06-12
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-02 01:15:44

Label at a glance#

ProductLBEL Defense Total Compact Suncreen SPF 50 For Face - Matte Finish
Active ingredientOCTINOXATE, OCTOCRYLENE, ZINC OXIDE
Label structure9 sections

Indications and 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.

Dosage and administration

Apply liberally and evenly 15 minutes before sun exposure. Reapply: after 40 minutes of swimming or sweating immediately after towel drying at least every 2 hours Children under 6 months of age: 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 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

OTC - ACTIVE INGREDIENT SECTION

OTC - PURPOSE SECTION

Active IngredientsPurpose
OCTINOXATE 7%Sunscreen
OCTOCRYLENE 5%Sunscreen
ZINC OXIDE 16.66%Sunscreen

Uses

INDICATIONS & USAGE SECTION

  • 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

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

Directions

DOSAGE & ADMINISTRATION SECTION

  • Apply liberally and evenly 15 minutes before sun exposure.
  • Reapply:
    • after 40 minutes of swimming or sweating
    • immediately after towel drying
    • at least every 2 hours
  • Children under 6 months of age: 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 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.

Other information

STORAGE AND HANDLING SECTION

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

Inactive ingredients

INACTIVE INGREDIENT SECTION

DIMETHICONE, ZEA MAYS (CORN) STARCH, POLYMETHYLSILSESQUIOXANE, POLYETHYLENE, HDI/TRIMETHYLOL HEXYLLACTONE CROSSPOLYMER, MICA, OZOKERITE, BUTYROSPERMUM PARKII (SHEA) BUTTER, SORBITAN SESQUIOLEATE, PEG/PPG-18/18 DIMETHICONE, PHENOXYETHANOL, TRIETHOXYCAPRYLYLSILANE, DIISOPROPYL ADIPATE, COPERNICIA CERIFERA (CARNAUBA) WAX, TOCOPHERYL ACETATE, CERAMIDE 3, CAPRYLYL GLYCOL, CHLORPHENESIN, PHYSALIS ANGULATA EXTRACT, FRAGRANCE, CAPRYLIC/CAPRIC TRIGLYCERIDE, SILICA, TRIMETHYLSILOXYSILICATE, OXOTHIAZOLIDINE, LINALOOL.

MAY CONTAIN: TITANIUM DIOXIDE, IRON OXIDES.

SPL UNCLASSIFIED SECTION

Dist. by Ventura Corp. Ltd.,
San Juan, Puerto Rico 00926.

PRINCIPAL DISPLAY PANEL - 9,5 g Container Box

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

MEDIUM

L'BEL
DÉFENSETOTAL

HIGH PROTECTION
SPF
50

compact cream sunscreen
for face - matte finish

BROAD SPECTRUM
WATER RESISTANT (40 minutes)

Net Wt. 0.34 oz. e (9,5 g)

PRINCIPAL DISPLAY PANEL - 9,5 g Container Box
PRINCIPAL DISPLAY PANEL - 9,5 g Container Box

FDA-Initiated Inactive NDC Indexing#

Products#

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

DailyMed product names page 1 of 1 · 29 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
43596-006243596-0062-1, 43596-0062-2

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 27 matching rows.

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
3237b6fa-9934-c59a-e063-6394a90a8e97fba77dd2-00e8-42b0-8b7d-7658596beef92025-04-07WarningsExact identifier
spl set id: fba77dd2-00e8-42b0-8b7d-7658596beef9

Reported adverse events (FAERS/openFDA)#

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