FDA.reportPublic FDA data

MELAO Roll-on Deodorant

Manufacturer
Guangzhou Yilong Cosmetics Co.,Ltd.
Effective date
2024-06-03
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 00:13:18

Label at a glance#

ProductMELAO Roll-on Deodorant
Active ingredientZINC PHENOLSULFONATE
Label structure11 sections

Indications and uses

Apply to underarm only and replace cap tightly after use.

Label contents#

Full prescribing information#

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Zinc Phenolsulfonate 2%

Purpose

OTC - PURPOSE SECTION

Deodorant

Uses

INDICATIONS & USAGE SECTION


Apply to underarm only and replace cap tightly after use.

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.

INACTIVE INGREDIENT SECTION

PARAFFIN
CETYL ALCOHOL
PEG-6 SORBITAN STEARATE
POLYSORBATE 60
WATER O-15

GLYCERIN
ETHYLHEXYL PALMITATE
XANTHAN GUM

DOSAGE & ADMINISTRATION SECTION


Apply to underarm only and replace cap tightly after use.
Do not apply to broken skin.Discontinue use if rash or irritation develops. Keep out
of reach of children.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabellabellabellabellabel

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
ZINC CATION Pharmacologic Class Indexing2Indexing - Pharmacologic Class20180813

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
f47a510b-6679-4664-b2d6-47b5c4afe7ccProduct name420260217
030ce964-9b2d-45aa-b5d3-f78ce03ef61cProduct name220250515
0306390c-dd77-4363-afe0-63c58088b2a1Product name120220120
503ea967-4b9c-48cf-9e87-c7975295849dProduct name220220120
190f2a5b-bbc8-65c7-fcb0-97891307b917Product name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
83566-295-01MELAO Roll-on Deodorant30 mL in 1 BOTTLE, PLASTICLIQUID303
83566-295-02MELAO Roll-on Deodorant30 mL in 1 BOTTLE, PLASTICLIQUID303
83566-295-03MELAO Roll-on Deodorant30 mL in 1 BOTTLE, PLASTICLIQUID303

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
83566-295MELAO ROLL-ON DEODORANT (ZINC PHENOLSULFONATE) LIQUID [GUANGZHOU YILONG COSMETICS CO.,LTD.]33 package rows20240606_16fdbb46-382f-ed9e-e063-6394a90ae5aa.zip

Products#

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

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
83566-29583566-295-01, 83566-295-02, 83566-295-03

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

Name, UNII, Kind table
NameUNIIKind
PARAFFINI9O0E3H2ZEIACT
CETYL ALCOHOL936JST6JCNIACT
PEG-6 SORBITAN STEARATE3453J8557NIACT
POLYSORBATE 60CAL22UVI4MIACT
WATER O-1563M8RYN44NIACT
ZINC PHENOLSULFONATE4O71YT5YB5ACTIB
GLYCERINPDC6A3C0OXIACT
ETHYLHEXYL PALMITATE2865993309IACT
XANTHAN GUMTTV12P4NEEIACT

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
1a0942a7-bcbe-0706-e063-6294a90a5c9e16fdbb46-382f-ed9e-e063-6394a90ae5aa2024-06-03WarningsExact identifier
spl id: 1a0942a7-bcbe-0706-e063-6294a90a5c9e
spl set id: 16fdbb46-382f-ed9e-e063-6394a90ae5aa

Reported adverse events (FAERS/openFDA)#

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