Daily Eclipse SPF 30 Untinted

Manufacturer
DermaMed Solutions, LLC | Trilogy Laboratories, LLC
Effective date
2020-02-10
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 23:41:28

Label at a glance#

ProductDaily Eclipse SPF 30 Untinted
Active ingredientZINC OXIDE, TITANIUM DIOXIDE
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredients

Titanium Dioxide, 7.5%

Zinc Oxide, 12%

OTC - PURPOSE SECTION

Purpose

Sunscreen

INDICATIONS & USAGE SECTION

Uses

Helps prevent sunburn

DOSAGE & ADMINISTRATION SECTION

Directions

  • Apply liberally 15 minutes before sun exposure.
  • Children under six months: Ask a doctor.
  • Reapply at least every 2 hours.
  • Use a water resistant sunscreen if swimming or sweating
  • Sun Protection Measures. Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease the risk, regularly use a sunscreen with Broad Spectrum SPF value of 15 or higher and other sun protection measures including:
  • limit time in the sun, especially from 10 am - 2 pm
  • Wear long-sleeved shirts, pants, hats, and sunglasses

INACTIVE INGREDIENT SECTION

Inactive ingredients

Aqua (water), Capric / Caprylic Triglycerides, Cetearyl Olivate and Sorbitan Olivate, Cimethicone (and) Dimethicone, Glycerin, Cyclopentasiloxane, Aloe Barbadensis, Vaccinium Vitis-idaea Fruit Extract (Lingostern), L- Ascorbic Acid, Camellia Sinensis (Green Tea) Leaf Extract, Phenoxyethanol, Ethylhexylglycerin, Fragrance (Natural)

WARNINGS SECTION

Warnings

For external use only

Do not use on damaged or broken skin

When using this product keep out of eyes. Rinse with water to remove.

Stop use and ask doctor if rash occurs

Keep out of reach of children. If product is swallowed, get medical help or contact a Poison Control Center right away.

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.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

FDA-Initiated Inactive NDC Indexing#

Products#

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

DailyMed product names page 1 of 1 · 18 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72492-00172492-001-01, 72492-001-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 16 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
c3e17225-4deb-97cf-e053-2a95a90ae0b472de6dd6-636d-30f4-e053-2991aa0a0ca72021-06-03WarningsExact identifier
spl set id: 72de6dd6-636d-30f4-e053-2991aa0a0ca7

Reported adverse events (FAERS/openFDA)#

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