FDA.reportPublic FDA data

MELAO Sunscreen Stick

Manufacturer
Guangdong Aimu Biological Technology Co., Ltd
Effective date
2025-06-25
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 01:05:45

Label at a glance#

ProductMELAO Sunscreen Stick
Active ingredientCERAMIDE NP, TOCOPHEROL, OCTOCRYLENE
Label structure11 sections

Indications and uses

Step1：Set off the cap before use Step2：Turn the roller and take an appropriate amount of cream Step3：Apply evenly to the body

Label contents#

Full prescribing information#

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Active ingredients 5%

CERAMIDE NP 2%

TOCOPHEROL 2%

Purpose

OTC - PURPOSE SECTION

sunscreen

Uses

INDICATIONS & USAGE SECTION


Step1：Set off the cap before use
Step2：Turn the roller and take an appropriate amount of cream
Step3：Apply evenly to the body

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

Turn the roller and take an appropriate amount of cream
Apply evenly to the body

Inactive ingredients

INACTIVE INGREDIENT SECTION

CYCLOPENTASILOXANE, CYCLOHEXASILOXANE, ETHYLHEXYL PALMITATE, OZOKERITE, MICROCRYSTALLINE WAX, DICAPRYLYL CARBONATE, THEOBROMA CACAO (COCOA) SEED BUTTER, SILICA, POLYMETHYLSILSESQUIOXANE, HOMOSALATE, ETHYLHEXYL METHOXYCINNAMATE, POLYGLYCERYL-2 TRIISOSTEARATE, BISABOLOL, PHENOXYETHANOL, AROMA

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
83566-188-01MELAO Sunscreen Stick15 g in 1 BOTTLESTICK152

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
83566-18883566-188-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Name, UNII, Kind table
NameUNIIKind
ETHYLHEXYL PALMITATE2865993309IACT
CERAMIDE NP4370DF050BACTIB
POLYGLYCERYL-2 TRIISOSTEARATE68DUY2D39AIACT
TOCOPHEROLR0ZB2556P8ACTIB
OCTOCRYLENE5A68WGF6WMACTIB

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
5ab9b09f-19df-73ec-e063-6394a90aba181ae6c49a-3861-29b3-e063-6394a90aa3232026-09-05WarningsExact identifier
spl set id: 1ae6c49a-3861-29b3-e063-6394a90aa323

Reported adverse events (FAERS/openFDA)#

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