Tinted Liplux

Manufacturer
Bell International Laboratories, Inc
Effective date
2021-07-21
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 22:39:53

Label at a glance#

ProductTinted Liplux
Active ingredientOCTISALATE, OCTOCRYLENE, AVOBENZONE
Label structure8 sections

Indications and uses

Helps prevent sunburn. If used as directed wtih 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 15 minutes before sun exposure & agan after 80 minutes of swimming or sweating. Apply at least every 2 hours. Sun Protection Measures - to decrease your risk of cancer and early skin aging, 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, especialyl from 10 a.m. to 2 p.m. and wear long-sleeved shirts, pants...

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Avobenzone 2.9%, Octisalate 4.9%, Octocrylene 7.6%

Purpose

OTC - PURPOSE SECTION

Sunscreens

Uses

INDICATIONS & USAGE SECTION

Helps prevent sunburn. If used as directed wtih 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. Do not use on damaged or broken skin. When using this product keep out of eyes. Stop use and ask doctor if skin 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

Apply liberally 15 minutes before sun exposure & agan after 80 minutes of swimming or sweating. Apply at least every 2 hours. Sun Protection Measures - to decrease your risk of cancer and early skin aging, 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, especialyl from 10 a.m. to 2 p.m. and wear long-sleeved shirts, pants, hats and sunglasses. Children under 6 months: Ask a doctor.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Acacia Senegal Gum, Aloe Barbadensis Leaf Extract, Astrocaryum Vulgare Kernel Oil (organic), Behenyl Behenate, Bisabolol (organic), Butyloctyl Salicylate, Calcium Sodium Borosilicate, Caprylic/Capric Triglyceride, Carthamus Tinctorium (Safflower) seed Oil, Citric Acid, Cocos Nucifers (Coconut) OIl (organic), Copernicia Cerifera (Carnuba) Wax (organic), Euphorbia Cerifera (Candelilla) Wax, Flavor, Heilianthus Annuus (Sunflower) Seed Oil (organic), Ipomoea Batatas Tuber Extract, Iron Oxides, Linoleic Acid, Maltodextrin, Octyldodecyl Oleate, Persea Gratissima (Avocado) Oil (organic), Phospholipids, Phytosterols, Polyhydroxystearic Acid, Raphanus Sativus (Raddish) Root Extract, Ricinus Communis (Castor) Seed Oil (organic), Rosa Canina Fruit Extract (orgnaic), Rosmarinus Officinals (Rosemary) Leaf Extract (orgnaic), Rubus Idaeus (Raspberry) Seed Oil (organic), Simmondsia Chinensis (Jojoba) Seed Oil (organic), Stevia Rebaudiana Extract, Tapioca Starch (organic), Tetrahexyldecyl Ascorbate, Theobroma Granfilorum Seed Butter (organic), Titanium Dioxide, Tocopherol (organic).

Other Information

OTHER SAFETY INFORMATION

Protect this product from excessive heat and direct sun.

Questions or Comments?

OTC - QUESTIONS SECTION

Call 760-940-2125

container primary and secondary label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
76150-31576150-315-32

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 36 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.

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Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
c7a34f35-0c2a-6dbf-e053-2995a90a4775c7a34f35-0c29-6dbf-e053-2995a90a47752021-07-21WarningsExact identifier
spl id: c7a34f35-0c2a-6dbf-e053-2995a90a4775
spl set id: c7a34f35-0c29-6dbf-e053-2995a90a4775

Reported adverse events (FAERS/openFDA)#

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