FDA.reportPublic FDA data

Melao Numb Spray

Manufacturer
Guangzhou Yilong Cosmetics Co., Ltd | Guangzhou Yilong Cosmetics Co.,Ltd.
Effective date
2024-07-25
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 20:58:03

Label at a glance#

ProductMelao NumbSpray
Active ingredientLIDOCAINE
Label structure10 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Lidocaine

OTC - PURPOSE SECTION

Soothing the pain of tattoos

INACTIVE INGREDIENT SECTION

Aqua

Alcohol

Polysorbate 20

Glycerin

Propylene Glycol

Yucca Glauca Root Extract

Achillea Millefolium Extract

Caprylyl Glycol

Disodium EDTA

Phenoxyethanol

Aroma

Citric Acid

Methylisothiazolinone

Sodium Metabisulfate

INDICATIONS & USAGE SECTION

1.Adults: When practical, cleanse the affected areawith mild soap and warm water and rinse thoroughly.Gently dry by patting or blotting with tissue or a softcloth before application of the product.

2. Apply exterally to the affected area up to 6 timesdaily.

3. Children under 12 years of age: consult a doctor.

WARNINGS SECTION

1. For external use only.

OTC - STOP USE SECTION

1. Stop use and ask a doctor if rash occurs.

OTC - WHEN USING SECTION

1. Do not use on damaged or broken skin.

DOSAGE & ADMINISTRATION SECTION

1. Adults: When practical, cleanse the affected area with mild soap and warm water and rinse thoroughly.Gently dry by patting or blotting with tissue or a softcloth before application of the product.

2. Apply exterally to the affected area up to 6 timesdaily.

3. Children under 12 years of age: consult a doctor.

OTC - DO NOT USE SECTION

1. Do not use on damaged or broken skin.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

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DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
83566-300MELAO NUMBSPRAY (LIDOCAINE) LIQUID [GUANGZHOU YILONG COSMETICS CO., LTD]1Unmatched20240728_1e0fe13a-3899-9f87-e063-6394a90a2fcb.zip

Products#

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

DailyMed product names page 1 of 1 · 16 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
83566-30083566-300-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 15 matching rows.

Name, UNII, Kind table
NameUNIIKind
YUCCA GLAUCA ROOT1A15YBH7N1IACT
SODIUM METABISULFITE4VON5FNS3CIACT
LIDOCAINE98PI200987ACTIB
CITRIC ACID ACETATEDSO12WL7AUIACT
ACHILLEA MILLEFOLIUM2FXJ6SW4PKIACT
GLYCERINPDC6A3C0OXIACT
PROPYLENE GLYCOL 1-(2-METHYLBUTYRATE)9Q5W5G6461IACT
CAPRYLYL GLYCOL00YIU5438UIACT
AROMADENDRIN7YA4640575IACT
ALCOHOL3K9958V90MIACT
WATER059QF0KO0RIACT
DISODIUM EDTA-COPPER6V475AX06UIACT
PHENOXYETHANOLHIE492ZZ3TIACT
POLYSORBATE 207T1F30V5YHIACT
METHYLISOTHIAZOLINONE229D0E1QFAIACT

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
3afa631a-3094-7771-e063-6394a90a1cd01e0fe13a-3899-9f87-e063-6394a90a2fcb2025-07-28WarningsExact identifier
spl set id: 1e0fe13a-3899-9f87-e063-6394a90a2fcb

Reported adverse events (FAERS/openFDA)#

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