Locana Zinc Oxide Sunscreen Broad Spectrum SPF 40

Manufacturer
Wabis Tokyo Inc.
Effective date
2021-04-02
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 22:47:55

Label at a glance#

ProductLocana Zinc Oxide Sunscreen Broad Spectrum SPF 40
Active ingredientZINC OXIDE
Label structure8 sections

Indications and uses

Helps prevent sun burn. 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 15 minutes before sun exposure. Sun Protection Measures.  Spending time in the sun increases your r isk 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. Limit time in the sun, especially from 10 a.m. – 2 p.m. Wear long-sleeved shirts, pants, hats, and sunglasses. Reapply at least every 2 h...

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Zinc Oxide: 24.5%

Purpose

OTC - PURPOSE SECTION

Sunscreen

Uses

INDICATIONS & USAGE SECTION

  • Helps prevent sun burn.
  • 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

Do not use

OTC - DO NOT USE SECTION

  • On damaged or broken skin.

When using this product

OTC - WHEN USING SECTION

  • Keep out of eyes. Rinse with water to remove.

Stop use and ask a doctor if

OTC - STOP USE SECTION

  • Rash occurs.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

  • Apply liberally 15 minutes before sun exposure.
  • Sun Protection Measures. Spending time in the sun increases your r isk 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.
  • Limit time in the sun, especially from 10 a.m. – 2 p.m.
  • Wear long-sleeved shirts, pants, hats, and sunglasses.
  • Reapply at least every 2 hours.
  • Use a water resistant sunscreen if swimming or sweating.
  • Children under 6 months of age: Ask a doctor.

Other information

SPL UNCLASSIFIED SECTION

  • Protect the product in this container from excessive heat and direct sun.
  • Store at 20–25°C (68–77°F)

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Dimethicone, Caprylic/Capric Triglyceride, Polyhydroxystearic Acid, 1, 2-Hexanediol, Dimethicone /PEG-10/15 Crosspolymer, Hydrogen Dimethicone, Butylene Glycol, Tremella Fuciformis Polysaccharide, Aleurites Moluccanus Seed Oil, Rosa Roxburghii Fruit Extract, Geranium Rober tianum Extract, Terminalia Ferdinandiana Fruit Extract, Symphytum Officinale Leaf Extract, Allantoin, Morinda Citrifolia Fruit Juice, Myrciaria Dubia Fruit Extract, Ascorbyl Glucoside, Niacinamide, Thymus Serpyllum Extract, Hydrolyzed Prunus Domestica, Cynara Scolymus (Artichoke) Leaf Extract, Rosa Centifolia Flower Oil, Hibiscus Sabdariffa Flower Extract, Alpinia Speciosa Leaf Extract, Chamomilla Recutita (Matricaria) Flower Extract, Passiflora Edulis Fruit Extract, Plantago Major Seed Extract, Melissa Officinalis Leaf Extract, Glucosyl Hesperidin, Citrus Reticulata (Tangerine) Peel Extract, Glycine Soja (Soybean) Seed Extract, Scutellaria Baicalensis Root Extract, Xanthophylls, Vaccinium Myrtillus Leaf Extract, Cyanocoba lamin, Glucosyl Ceramide, Alpha-Glucan, Glycerin, Phytosterols, Hydrogenated Lecithin, Tocopherol, Zea Mays (Corn) Oil, Car thamus Tinctorius (Safflower) Seed Oil, Isostearic Acid, Sodium Chloride

Questions or comments?

OTC - QUESTIONS SECTION

Call 302-295-5078 Monday – Friday (9 a.m. – 5 p.m. CST)

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Outer PackageOuter PackageInner PackageInner Package

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
81720-10081720-100-01

Ingredients#

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DailyMed ingredient rows page 1 of 2 · 43 matching rows.

Source Document#

Source XML

openFDA label cross-check#

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Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
ce62de7d-9f29-8f33-e053-2a95a90a7dbcbefd6f29-8bf8-fa1a-e053-2995a90af08d2021-10-15WarningsExact identifier
spl set id: befd6f29-8bf8-fa1a-e053-2995a90af08d

Reported adverse events (FAERS/openFDA)#

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