FDA.reportPublic FDA data

MELAO TALLOW SUNSCREEN

Manufacturer
Guangzhou Haishi Biological Technology Co., Ltd.
Effective date
2026-05-12
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 01:56:48

Label at a glance#

ProductMELAO TALLOW SUNSCREEN
Active ingredient.BETA.-BISABOLOL, TALLOW ACID, BEEF, ETHYL METHOXYCINNAMATE, SAURURUS CHINENSIS FLOWER, STEPHANIA TETRANDRA WHOLE, PEG-9 DIGLYCIDYL ETHER/SODIUM HYALURONATE CROSSPOLYMER, TOCOPHERYL RETINOATE
Label structure11 sections

Indications and uses

Step1: After using the basic lotion Step2: Apply appropriate amount to the palm, smear on the whole face, neck and other easily exposed parts Step3: Apply evenly and gently so that it absorbs into a film

Label contents#

Full prescribing information#

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

ETHYLHEXYL METHOXYCINNAMATE 4%

SODIUM HYALURONATE 0.2%
BISABOLOL 0.3%
ADEPS BOVIS 5%
TOCOPHERYL ACETATE 1%

SAURURUS CHINENSIS LEAF/ROOT EXTRACT 2%
STEPHANIA TETRANDRA EXTRACT 0.1%

Purpose

OTC - PURPOSE SECTION

sunscreen

Uses

INDICATIONS & USAGE SECTION

Step1: After using the basic lotion
Step2: Apply appropriate amount to the palm, smear on the whole face, neck and other easily exposed parts
Step3: Apply evenly and gently so that it absorbs into a film

Warnings

WARNINGS SECTION

For external use only.

Stop use and ask a doctor if

OTC - STOP USE SECTION

rash occurs.

Do not use

OTC - DO NOT USE SECTION

on damaged or broken skin.

When using this product

OTC - WHEN USING SECTION

keep out of eyes. Rinse with water to remove.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away.

Dosage

DOSAGE & ADMINISTRATION SECTION

Squeeze out an appropriate amount of sunscreen and spread evenly on skin.

Inactive ingredients

INACTIVE INGREDIENT SECTION

WATER 67.6%
PROPYLENE GLYCOL 4%
GLYCERIN 4%
ALLANTOIN 0.3%
DIMETHICONE 1%
CETEARYL GLUCOSIDE 1%
CETETH-21 0.8%
CETETH-2 1.3%
CETEARYL ALCOHOL 1.5%
CARBOMER 0.3%
TRIETHANOLAMINE 0.3%
PHENOXYETHANOL 0.4%
ETHYLHEXYLGLYCERIN 0.1%
TARAXACUM OFFICINALE (DANDELION) LEAF EXTRACT 0.8%

ETHYLHEXYL SALICYLATE 4%

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-136952243219562GTIN-13: 6952243219562
EAN-13: 6952243219562
GTIN storage (14 digits): 06952243219562		01.jpg

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
60771-0001-1MELAO TALLOW SUNSCREEN60 g in 1 JARCREAM603

Products#

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

DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
60771-000160771-0001-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 matching rows.

Name, UNII, Kind table
NameUNIIKind
.BETA.-BISABOLOLLP618AV2EAACTIB
DIPROPYLENE GLYCOLE107L85C40IACT
ALLANTOIN344S277G0ZIACT
GLYCERINPDC6A3C0OXIACT
TALLOW ACID, BEEF5U9XZ261ERACTIB
ETHYL METHOXYCINNAMATESD418S06XDACTIB
SAURURUS CHINENSIS FLOWER9L0SCP0SKZACTIB
STEPHANIA TETRANDRA WHOLE7S7TV2F4XCACTIB
PEG-9 DIGLYCIDYL ETHER/SODIUM HYALURONATE CROSSPOLYMER788QAG3W8AACTIB
TOCOPHERYL RETINOATE0WN694NBMMACTIB

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
MELAO TALLOW SUNSCREENETHYLHEXYL METHOXYCINNAMATEGuangzhou Haishi Biological Technology Co., Ltd.22982b28-37df-ed81-e063-6394a90a77db2026-05-12WarningsExact identifier
ndc (package): 60771-0001-1
ndc (product): 60771-0001
ndc11 (package): 60771000101
spl id: 519cf0bd-738a-cd84-e063-6294a90ab373
spl set id: 22982b28-37df-ed81-e063-6394a90a77db

Reported adverse events (FAERS/openFDA)#

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