OUHOE Bean Sunscreen

Manufacturer
Shantou Ouhoe Technology Co., Ltd.
Effective date
2025-12-26
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:28:41

Label at a glance#

ProductOUHOE Bean Sunscreen
Active ingredientTRITICUM VULGARE (WHEAT) GERM OIL, GLYCINE SOJA (SOYBEAN) OIL UNSAPONIFIABLES
Label structure12 sections

Storage and handling

Store in a cool and dry place.

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

GLYCINE SOJA (SOYBEAN) EXTRACT、TRITICUM VULGARE (WHEAT) PROTEIN

OTC - PURPOSE SECTION

1. It can provide double protection, effective sun protection and deep moisturizing, providing all-weather skin protection.

2. It has broad-spectrum protection, contains UVA and UVB filters, and effectively prevents sunburn.

3. It can control oil while protecting against the sun, making your skin more refreshing.

4. It has a light texture, is easy to apply, and is convenient and quick to use. It is an ideal choice for sunscreen products.

OTC - WHEN USING SECTION

1.15-20 minutes before going out, apply the sunscreen evenly on the face or body where the sunscreen is required, massage until fully absorbed, and then form a film naturally.
2.If you need to apply makeup, please use it before makeup. If exposed to the sun for a long time, it needs to be reapplied every 2-3 hours.

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.

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.

STORAGE AND HANDLING SECTION

Store in a cool and dry place.

INACTIVE INGREDIENT SECTION

AQUA、ETHYLHEXYL METHOXYCINNAMATE、TITANIUM DIOXIDE、ISONONYL ISONONANOATE、GLYCERYL STEARATE

INDICATIONS & USAGE SECTION

1.15-20 minutes before going out, apply the sunscreen evenly on the face or body where the sunscreen is required, massage until fully absorbed, and then form a film naturally.
2.If you need to apply makeup, please use it before makeup. If exposed to the sun for a long time, it needs to be reapplied every 2-3 hours.

DOSAGE & ADMINISTRATION SECTION

1.15-20 minutes before going out, apply the sunscreen evenly on the face or body where the sunscreen is required, massage until fully absorbed, and then form a film naturally.
2.If you need to apply makeup, please use it before makeup. If exposed to the sun for a long time, it needs to be reapplied every 2-3 hours.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
Data codeCode 128OU-A05-0587-01OU-A05-0587-01.jpg

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
85163-018-01OUHOE Bean Sunscreen50 mg in 1 BOTTLE, PLASTICCREAM501

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
85163-01885163-018-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 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
OUHOE Bean SunscreenTITANIUM DIOXIDEShantou Ouhoe Technology Co., Ltd.46d3b11f-93d9-0e38-e063-6294a90a41c32025-12-26WarningsExact identifier
ndc (package): 85163-018-01
ndc (product): 85163-018
ndc11 (package): 85163001801
spl id: 46d3b11f-93da-0e38-e063-6294a90a41c3
spl set id: 46d3b11f-93d9-0e38-e063-6294a90a41c3

Reported adverse events (FAERS/openFDA)#

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