LiProtect SPF 35

Manufacturer
Science of Skincare | Micro Connection Enterprises INC | West Coast Cosmetics
Effective date
2021-04-01
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 22:49:41

Label at a glance#

ProductLiProtect SPF 35
Active ingredientZINC OXIDE, TITANIUM DIOXIDE
Label structure13 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Zinc Oxide 10.2%

Titanium Dioxide 1.0%

OTC - PURPOSE SECTION

Sunscreen

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 AND PRECAUTIONS SECTION

For external use only.

OTC - DO NOT USE SECTION

Do not use on damaged or borken 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.

DOSAGE & ADMINISTRATION SECTION

Apply liberally 15 minutes before sun exposure

Use a water resistance sunscreen if swimming or sweating.

Reapply at least every 2 hours

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 board spectrum SPF of 15 or higher and other sun protection measures including: limit time in sun, especially from 10am to 2pm. wear long-sleeve shirts, pants, hats, and sunglasses. Children under the age of 6 months. Ask a doctor.

OTHER SAFETY INFORMATION

Protect this product from excessive heat and direct sun.

Store at 20-25C (68 - 77F)

OTC - QUESTIONS SECTION

Call Customer Care at (888) 804 - 4447

INACTIVE INGREDIENT SECTION

Vegetable Oil, Cocos Nucifera (Coconut) Oil, Euphorbia Cerifera (Candelilla) Wax, Flavor(Aroma), C12-15 Alkyl Benzoate, Ozokerite, Hydrogenated Vegetable Oil, Sambucus Nigra Fruit Extract, Tocopherol, VP/Eicosene Copolymer, Caprylic/Capric Triglyceride, Dipalmitoyl Hydroxyproline, Simmondsia Chinensis (Jojoba) Seed Oil, Glycine Soja (Soybean) Oil, Polyhydroxystearic Acid, Ethylhexyl Palmitate, Rebaudioside A, Aluminum Stearate, Tribehenin, Palmitoyl Tripeptide-1, Linoleic Acid, Isostearic Acid, Glycine Soja (Soybean) Sterols, Phospholipids, Sorbitan Isostearate, Alumina.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

69219-109 bottle69219-109 bottle69219-109 bottle add-on label69219-109 bottle add-on label69219-109 box69219-109 box

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
69219-10969219-109-01, 69219-109-11

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
0ce665f4-3e47-7403-e063-6394a90a9becb69c1659-0a3f-3379-e053-2995a90ad06f2023-12-19WarningsExact identifier
spl set id: b69c1659-0a3f-3379-e053-2995a90ad06f

Reported adverse events (FAERS/openFDA)#

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