FDA.reportPublic FDA data

MELAO ZINC STICK(YELLOW)

Manufacturer
Guangzhou Haishi Biological Technology Co., Ltd.
Effective date
2026-08-24
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
daily-update
Hydrated at
2026-08-26 01:01:43

Label at a glance#

ProductMELAO zinc stick(YELLOW)
Active ingredientZINC OXIDE, OCTOCRYLENE
Label structure11 sections

Dosage and administration

Apply evenly and generously to exposed skin 15-20 minutes before sun exposure. Do not rub in. Reapply every 2 hours, or immediately after swimming, sweating or toweling. Limiting sun exposure, wearing protective clothing, and using sunscreen are all part of effective sun protection.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

TITANIUM DIOXIDE 2.4%

ZINC OXIDE 2%

OCTOCRYLENE 2%

Purpose

OTC - PURPOSE SECTION

Sunscreen

Use

INDICATIONS & USAGE SECTION

Helps prevent sunburn

Warnings

WARNINGS SECTION

For external use only.

Do not use

OTC - DO NOT USE SECTION

on damaged or broken skin.

Stop use and ask a doctor if

OTC - STOP USE SECTION

rash occurs.

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

Directions

DOSAGE & ADMINISTRATION SECTION

Apply evenly and generously to exposed skin 15-20 minutes before sun exposure.
Do not rub in.
Reapply every 2 hours, or immediately after swimming, sweating or toweling.
Limiting sun exposure, wearing protective clothing, and using sunscreen are all part of effective sun protection.

Inactive ingredients

INACTIVE INGREDIENT SECTION

MICA,SYNTHETIC WAX,SQUALANE,ETHYLHEXYL PALMITATE,MINERAL OIL,CI 19140,ALUMINUM HYDROXIDE,ISOHEXADECANE,OZOKERITE,ISONONYL ISONONANOATE,CI 77491

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LABELLABEL

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-136952243228595GTIN-13: 6952243228595
EAN-13: 6952243228595
GTIN storage (14 digits): 06952243228595		00.jpg

Products#

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

DailyMed product names page 1 of 1 · 24 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
60771-005160771-0051-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 22 matching rows.

Name, UNII, Kind table
NameUNIIKind
ZINC OXIDESOI2LOH54ZACTIB
OCTOCRYLENE5A68WGF6WMACTIB
MICAV8A1AW0880IACT
SYNTHETIC WAX (1200 MW)Q3Z4BCH099IACT
SQUALANEGW89575KF9IACT
ETHYLHEXYL PALMITATE2865993309IACT
MINERAL OILT5L8T28FGPIACT
CI 19140I753WB2F1MIACT
ALUMINUM HYDROXIDE5QB0T2IUN0IACT
ISOHEXADECANE918X1OUF1EIACT
CERESINQ1LS2UJO3AIACT
ISONONYL ISONONANOATES4V5BS6GCXIACT
CI 774911K09F3G675IACT
SILICAETJ7Z6XBU4IACT
TRIETHOXYCAPRYLYLSILANELDC331P08EIACT
BEESWAX2ZA36H0S2VIACT
CYCLOPENTASILOXANE0THT5PCI0RIACT
DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (SOFT PARTICLE)9E4CO0W6C5IACT
MICROCRYSTALLINE WAXXOF597Q3KYIACT
BHT1P9D0Z171KIACT
CI 7789115FIX9V2JPIACT
PHENOXYETHANOLHIE492ZZ3TIACT

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 zinc stick(YELLOW)TITANIUM DIOXIDE,ZINC OXIDE,OCTOCRYLENEGuangzhou Haishi Biological Technology Co., Ltd.59c3009b-ae16-52e1-e063-6394a90a69ee2026-08-24WarningsExact identifier
ndc (package): 60771-0051-1
ndc (product): 60771-0051
ndc11 (package): 60771005101
spl id: 59c3009b-ae17-52e1-e063-6394a90a69ee
spl set id: 59c3009b-ae16-52e1-e063-6394a90a69ee

Reported adverse events (FAERS/openFDA)#

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