DreamBeam Sunscreen Sunlit

Manufacturer
Kosas Cosmetics, LLC
Effective date
2025-02-13
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 00:55:12

Label at a glance#

ProductDreamBeam Sunscreen Sunlit
Active ingredientZINC OXIDE
Label structure8 sections

Dosage and administration

Directions: Apply liberally 15 minutes before sun exposure Children under 6 months of age: ask a doctor Sun Protection Measures: Spending time in the sun increases your risk of skin cancer and early skin aging. 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 10am - 2pm, wear long-sleeve...

Label contents#

Full prescribing information#

Directions

DOSAGE & ADMINISTRATION SECTION

Directions:
Apply liberally 15 minutes before sun exposure
Children under 6 months of age: ask a doctor

Sun Protection Measures:

Spending time in the sun
increases your risk of skin cancer and early skin aging.
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 10am - 2pm, wear long-sleeved shirts, pants, hats, and sunglasses, and reapply after 80 minutes of swimming or sweating, immediately after towel drying, at least every 2 hours

Warnings

WARNINGS SECTION

Warnings:
For external use only
When using this product keep out of eyes. Rinse with water to remove.
Stop use and ask a doctor if rash occurs.
Keep out of reach of children. If swallowed, get medical
help or contact a Poison Control Center right away.

Do not use on damaged or broken skin.

INACTIVE INGREDIENT SECTION

OuterOuter

Use

INDICATIONS & USAGE SECTION

Uses:

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.

Keep out of reach of children

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.

Purpose

OTC - PURPOSE SECTION

Sunscreen

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

TubeTube

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

OuterOuter

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
f52be47f-7aa7-46c0-b1fa-50c18dd50206Product name120201029
444b3e50-f226-46ef-bfca-2e7035d140cdProduct name120190611
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
597b1cfd-7b31-5048-62be-ca5cd740da2fProduct name120140508
ec2149b3-5c6d-5344-f757-c86411073075Product name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
82554-103-40DreamBeam Sunscreen Sunlit1 in 1 BOXLOTION13
82554-103-40DreamBeam Sunscreen Sunlit40 mL in 1 TUBELOTION403

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
82554-103DREAMBEAM SUNSCREEN SUNLIT (SUNSCREEN ZINC OXIDE) LOTION [KOSAS COSMETICS, LLC]3Current NDC, 2 package rows20250215_2e093b82-2a36-cc0f-e063-6394a90a4d6d.zip

Products#

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

DailyMed product names page 1 of 1 · 39 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
82554-10382554-103-40

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 37 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
DreamBeam Sunscreen SunlitSUNSCREEN ZINC OXIDEKosas Cosmetics, LLC2e093b82-2a36-cc0f-e063-6394a90a4d6d2025-02-13WarningsExact identifier
ndc (package): 82554-103-40
ndc (product): 82554-103
ndc11 (package): 82554010340
spl id: 2e093b82-2a37-cc0f-e063-6394a90a4d6d
spl set id: 2e093b82-2a36-cc0f-e063-6394a90a4d6d

Reported adverse events (FAERS/openFDA)#

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