FDA.reportPublic FDA data

MELAO PIERCING AFTERCARE SPRAY

Manufacturer
Guangzhou Yilong Cosmetics Co., Ltd
Effective date
2024-08-08
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 20:57:00

Label at a glance#

ProductMELAO PIERCING AFTERCARE
Active ingredientPANTHENOL, SEA SALT
Label structure11 sections

Indications and uses

Step 1: Clean and thoroughly dry your skin. Step 2: Press the spray on the skin surface or other required areas.

Label contents#

Full prescribing information#

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Sea Salt 6%

Panthenol 3.60%

-Inactive ingredients

INACTIVE INGREDIENT SECTION

Water 55%

Glycerin Propylene Glycol 8%

Saururus Chinensis Leaf/Root Extiact 5%

Taraxacum Officinale (Dandelion) Leaf Extract 5%

Aloe Barbadensis Leaf Extract 4.5%

Erythritol 3.70%

Melaleuca Alternifolia (Tea Tree) Leaf Oil 2.40%

Rosmarinus Oficinalis (Rosemary) Extract 2.30%

Tocopherol 2%

Hydroxyacetophenone 1%

1,2-Hexanediol 0.90%

Allantoin 0.07%

Dipotassium Glycyrrhizate 0.03%

Disodium EDTA 0.5%

Purpose

OTC - PURPOSE SECTION

Post perforation care

Uses

INDICATIONS & USAGE SECTION

Step 1: Clean and thoroughly dry your skin.
Step 2: Press the spray on the skin surface or other required areas.

Warning

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 withwater to remove.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

DOSAGE & ADMINISTRATION

DOSAGE & ADMINISTRATION SECTION

DOSAGE & ADMINISTRATION

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LABELLABEL

Products#

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

DailyMed product names page 1 of 1 · 18 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
83566-57383566-573-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 16 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALLANTOIN344S277G0ZIACT
ERYTHRITOLRA96B954X6IACT
ROSMARINUS OFFICINALIS FLOWERING TOP OILOXN0D3N28LIACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
1,2-HEXANEDIOLTR046Y3K1GIACT
2'-HYDROXYACETOPHENONE3E533Z76W0IACT
GOSSYPIUM BARBADENSE LEAF251DUP3OSNIACT
PANTHENOLWV9CM0O67ZACTIB
ECHINACEA PURPUREA FLOWERING TOP WATERG72P70SL42IACT
GLYCERIN 1,2-DIMETHYL ETHER21JG3RIJ74IACT
TARAXACUM OFFICINALE LEAF0022LFJ74YIACT
MELALEUCA ALTERNIFOLIA LEAFG43C57162KIACT
DIPOTASSIUM GLUCARATEU9GJZ222NUIACT
MAGNESIUM DISODIUM EDTANDT563S5VZIACT
SEA SALT87GE52P74GACTIB
SAURURUS CHINENSIS WHOLE6DRV3D37XSIACT

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
269da965-c9e0-29dc-e063-6394a90a8a761f27e274-a2c0-ba5c-e063-6394a90abfe32024-11-11WarningsExact identifier
spl set id: 1f27e274-a2c0-ba5c-e063-6394a90abfe3

Reported adverse events (FAERS/openFDA)#

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