LASPA

Manufacturer
Vegewax Candleworx Ltd
Effective date
2021-11-30
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 22:25:16

Label at a glance#

ProductLASPA
Active ingredientZINC OXIDE
Label structure13 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Zinc Oxide 15%

OTC - PURPOSE SECTION

Sunscreen

INDICATIONS & USAGE SECTION

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 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.

INSTRUCTIONS FOR USE SECTION

Directions

• apply generously and evenly 15 minutes before sun exposure.

• children under 6 months of age: Ask a doctor.

• use a water resistance sunscreen if swimming or sweating

• reapply:

• immediately after towel drying.

• 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 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 SAFETY INFORMATION

Other information

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

• for further information please call 1-877-476-2758

INACTIVE INGREDIENT SECTION

Inactive ingredients

Water, Helianthus Annuus (Sunflower) Seed Oil*, Glycerin, Glyceryl Stearate, Vitis Vinifera (Grape) Seed Oil, Cetearyl Alcohol, Sorbitan Sesquioleate, Crambe Abyssinica Seed Oil, Glyceryl Caprylate, Butyrospermum Parkii (Shea) Butter, Tocopherol, Xanthan Gum, Glyceryl Undecylenate, Iron Oxides

*Certified Organic

125 mL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

50g

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Principal Display Panel - 50 mLPrincipal Display Panel - 50 mL

Products#

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

DailyMed product names page 1 of 1 · 17 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
44114-52044114-520-50, 44114-520-12

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 15 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
d20c8fe9-2ee9-edad-e053-2995a90a2364c3e257cd-a4af-63d6-e053-2a95a90a6eec2021-11-30WarningsExact identifier
spl id: d20c8fe9-2ee9-edad-e053-2995a90a2364
spl set id: c3e257cd-a4af-63d6-e053-2a95a90a6eec

Reported adverse events (FAERS/openFDA)#

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