FDA.reportPublic FDA data

Sunlight Daily Facial Moisturizing Sunscreen

Manufacturer
Crunchi LLC
Effective date
2020-11-20
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-05-31 23:34:00

Label at a glance#

ProductSunlight Daily Facial Moisturizing Sunscreen
Active ingredientZINC OXIDE
Label structure8 sections

Indications and 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.

Dosage and administration

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. 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. to 2 p.m. Wear long-sleeved...

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Zinc Oxide 15%** Sunscreen

Uses

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

WARNINGS SECTION

  • 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 a doctor if rash occurs.
  • Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

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. 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. to 2 p.m.
  • Wear long-sleeved shirts, pants, hats and sunglasses.
  • Re-apply at least every 2 hours.
  • Use a water resistant sunscreen if swimming or sweating.

Other Information

OTHER SAFETY INFORMATION

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

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water (Aqua), Glycerin*, Calophyllum inophyllum (Tamanu) Seed Oil*, Propsnediol, Aloe Barbadensis (Aloe Vera) Leaf Juice*, Jojoba Esters, Disteardimonium Hectorite, Polyglyceryl-2 Isostearate, Polyglyceryl-6 Polyricinloeate, Caprylic/capric Triglyceride, Sesamum Indicum (Sesame) Seed Oil*, Polyhydroxystearic Acid, Tocopherol, Citrus Sinsnsis (Sweet Oralge) Peel Oil*, Euterpe Oleracea (Acai) Pulp Powder*, Lycium Chinense (Goji) Fruit*, Rosmarinus Officinalis (Rosemary) Leaf Powder*, Phenethyl Alcohol, Ethylhexylglycerin

*Certified Organic Ingredients

**Non-nanoparticle

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Package LabelPackage Label

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
72444-0130-12022-01-28C16284748780-1d6a99b39-6540-a426-e053-dadaa90af4c2Crunchi

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72444-0130-1Sunlight Daily Facial Moisturizing Sunscreen30 mL in 1 BOXLOTION304

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
72444-0130SUNLIGHT DAILY FACIAL MOISTURIZING SUNSCREEN (SUNSCREEN) LOTION [CRUNCHI LLC]4Legacy NDC, 1 package rows20201121_70bfc4cd-7ea7-1d03-e053-2991aa0a5660.zip

Products#

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

DailyMed product names page 1 of 1 · 4 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72444-013072444-0130-1

Ingredients#

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

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

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
ZINC OXIDESOI2LOH54ZACTIB

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
b4912b1d-71d6-40ac-e053-2995a90a449f70bfc4cd-7ea7-1d03-e053-2991aa0a56602020-11-20WarningsExact identifier
spl id: b4912b1d-71d6-40ac-e053-2995a90a449f
spl set id: 70bfc4cd-7ea7-1d03-e053-2991aa0a5660

Reported adverse events (FAERS/openFDA)#

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