WOODSLEEP Tallow Sunscreen

Manufacturer
Shantou Woodsleep Biotechnology Co., Ltd.
Effective date
2025-11-26
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 01:18:23

Label at a glance#

ProductWOODSLEEP Tallow Sunscreen
Active ingredientTALLOW
Label structure10 sections

Storage and handling

Store in a cool and dry place.

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

TALLOW

OTC - WHEN USING SECTION

Apply evenly 15 minutes before sun exposure.
Reapply every 2 hours for prolonged protection.

Gently blend onto face and body.

OTC - PURPOSE SECTION

Sunscreen barrier: fully blocks UV rays and protects skin health.
Deep moisturizing: prevents dryness and keeps skin moisturized.
Sports adaptability: swimming and fitness without makeup removal, more lasting protection.
Lightweight and comfortable: silky and fits the skin, no burden to the touch.
Suitable for daily commuting, can be used alone or as a primer before makeup.
Mild formula reduces irritation, sensitive skin friendly.
Improves skin smoothness and soft touch.
Light texture, does not clog pores.
Suitable for a variety of skin types and skin tones, easy to control.
Re-application does not rub mud, convenient and not embarrassing.
Balance the water and oil status of the skin to avoid drying.
Reduce the loss of protective power caused by the external environment.
Natural nude makeup effect, no fake face and no oily shine.
Portable packaging design, worry-free re-application anytime, anywhere.
Strengthen the skin's ability to resist daily environmental pressure.

OTC - DO NOT USE SECTION

Discontinue use if signs of irritation or rash occur.

OTC - STOP USE SECTION

Discontinue use if signs of irritation or rash occur.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Please keep out of reach of children. Do not swallow.

WARNINGS SECTION

Please keep out of reach of children. Do not swallow.Please clean your hands before use to ensure the best results from the product. Discontinue use if signs of irritation or rash occur. Store in a cool and dry place.

INACTIVE INGREDIENT SECTION

AQUA、LAURYL PEG-8 DIMETHICONE、ETHYLHEXYL METHOXYCINNAMATE、TITANIUM DIOXIDE、PEG-10 GLYCERYL STEARATE

STORAGE AND HANDLING SECTION

Store in a cool and dry place.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
Data codeCode 128WO-A06-0071-01WO-A06-0071-01.jpg

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
85053-002-01WOODSLEEP Tallow Sunscreen57 mg in 1 BOXCREAM572

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
85053-00285053-002-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 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
WOODSLEEP Tallow SunscreenTITANIUM DIOXIDEShantou Woodsleep Biotechnology Co., Ltd.330a9f2e-7ce1-f83f-e063-6394a90a184a2025-11-26WarningsExact identifier
ndc (package): 85053-002-01
ndc (product): 85053-002
ndc11 (package): 85053000201
spl id: 448bdbfa-2de6-fce8-e063-6394a90a2cf7
spl set id: 330a9f2e-7ce1-f83f-e063-6394a90a184a

Reported adverse events (FAERS/openFDA)#

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