HANCHOBIT Sunscreen

Manufacturer
HANCHOYEANBIOTEC Co.,Ltd.
Effective date
2025-11-27
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 01:18:34

Label at a glance#

ProductHANCHOBIT Sunscreen
Active ingredientBETULA ALBA JUICE
Label structure12 sections

Storage and handling

Store in a cool and dry place.

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

BETULA ALBA JUICE

OTC - PURPOSE SECTION

1. Effectively resist UV damage, reduce external environmental irritation to the skin, and keep the skin healthy.

2. Lightweight texture quickly absorbed, non-sticky, and continuously provides moisturizing feeling.

3. Combines moisturizing and sunscreen dual effects, suitable for outdoor or daily use, helping the skin stay away from dryness and environmental damage.

OTC - WHEN USING SECTION

1. Clean the skin and keep it dry.

2. Take an appropriate amount of this product and apply it evenly on the face, body and other skin areas that need sun protection, and then wait for it to be absorbed.

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、TITANIUM DIOXIDE、ETHYLHEXYL METHOXYCINNAMATE、ISONONYL ISONONANOATE、GLYCERYL STEARATE、HYALURONIC ACID

INDICATIONS & USAGE SECTION

1. Clean the skin and keep it dry.

2. Take an appropriate amount of this product and apply it evenly on the face, body and other skin areas that need sun protection, and then wait for it to be absorbed.

DOSAGE & ADMINISTRATION SECTION

1. Clean the skin and keep it dry.

2. Take an appropriate amount of this product and apply it evenly on the face, body and other skin areas that need sun protection, and then wait for it to be absorbed.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
85164-005-01HANCHOBIT Sunscreen50 mg in 1 BOTTLE, PLASTICCREAM502

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
85164-00585164-005-01

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

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
12025-11-07monthly-update2026-06-03 17:39:35

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
HANCHOBIT SunscreenTITANIUM DIOXIDEHANCHOYEANBIOTEC Co.,Ltd.42fd5d3e-4e98-86d7-e063-6294a90a45c22025-11-27WarningsExact identifier
ndc (package): 85164-005-01
ndc (product): 85164-005
ndc11 (package): 85164000501
spl id: 449ff8f8-fe08-7bce-e063-6394a90ace56
spl set id: 42fd5d3e-4e98-86d7-e063-6294a90a45c2

Reported adverse events (FAERS/openFDA)#

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