silk SPF facial sunscreen fluid hybrid broad spectrum SPF 30 UVA/UVB

Manufacturer
OneKind.25
Effective date
2025-06-12
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-06-01 01:03:00

Label at a glance#

Productsilk SPF facial sunscreen fluid hybrid broad spectrum SPF 30 UVA/UVB
Active ingredientZINC OXIDE, HOMOSALATE
Label structure12 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredients

Zinc Oxide 10.5%

Homosalate 10%

OTC - PURPOSE SECTION

Purpose

Sunscreen

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.

WARNINGS SECTION


Warnings
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.

DOSAGE & ADMINISTRATION SECTION


Directions
Apply generously 15 minutes before sun
exposure. Reapply at least every 2 hours.
Use a water-resistant sunscreen if
swimming or sweating.

OTHER SAFETY INFORMATION


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. Children under 6
months of age: ask a doctor.

INACTIVE INGREDIENT SECTION


Inactive Ingredients
water/aqua/eau, caprylic/capric
triglyceride, glyceryl stearate se, coconut
alkanes, glycerin, coco-caprylate/caprate,
decyl glucoside, oryza sativa (rice) starch,
musa sapientum (banana) flower extract,
polyhydroxystearic acid, polyglyceryl-3
polyricinoleate, isostearic acid, lecithin,
xanthan gum, hydroxyethylcellulose,
caprylyl glycol, caprylhydroxamic acid,
sodium benzoate, citric acid, disodium
phosphate, sodium phosphate.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

CODSilkSPF30CODSilkSPF30

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
726062af-1135-4707-a1d7-57256991bbf9Product name220250226
19c71a3d-ed9c-166b-a7e5-38c250c35631Product name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
79356-202-01silk SPF facial sunscreen fluid hybrid broad spectrum SPF 30 UVA/UVB48 g in 1 TUBECREAM484
79356-202-02silk SPF facial sunscreen fluid hybrid broad spectrum SPF 30 UVA/UVB1 in 1 CARTONCREAM14

Products#

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

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
79356-20279356-202-01, 79356-202-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 23 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
silk SPF facial sunscreen fluid hybrid broad spectrum SPF 30 UVA/UVBZINC OXIDE AND HOMOSALATEOneKind.25d739bc43-d76e-9258-e053-2a95a90a3d2c2025-06-12WarningsExact identifier
ndc (package): 79356-202-01
ndc (package): 79356-202-02
ndc (product): 79356-202
ndc11 (package): 79356020201
ndc11 (package): 79356020202
spl id: 3765236c-138d-366f-e063-6294a90ac76a
spl set id: d739bc43-d76e-9258-e053-2a95a90a3d2c

Reported adverse events (FAERS/openFDA)#

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