Miami Beach Burn Relief

Manufacturer
Miami Beach Brands Corporation
Effective date
2016-12-20
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 01:21:00

Label at a glance#

ProductMiami Beach Burn Relief
Active ingredientLIDOCAINE HYDROCHLORIDE
Label structure7 sections

Dosage and administration

Adults and children two-years of age or older:  apply to affected area not more than three to four times daily. Children under two-years of age:  consult a physician.

Storage and handling

store at room temperature

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Lidocaine HCL  1.00%

Purpose

OTC - PURPOSE SECTION

Topical Pain Reliever

Indications:

INDICATIONS & USAGE SECTION

For the temporary relief of pain and itching due to sunburn, minor burns, insect bites, cuts and scrapes

Warnings:

WARNINGS SECTION

  • For external use only

OTC - DO NOT USE SECTION

  • Do not use in large quantities, particularly over raw or blistered areas.

OTC - STOP USE SECTION

  • If symptoms persist for more than seven days, discontinue use and consult physician.
  • ​Avoid contact with eyes.  ​Rinse well if contact occurs.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, consult physician.

Directions:

DOSAGE & ADMINISTRATION SECTION

  • Adults and children two-years of age or older:  apply to affected area not more than three to four times daily.
  • Children under two-years of age:  consult a physician.

Additional Information:

STORAGE AND HANDLING SECTION

store at room temperature

Inactive Ingredients:

INACTIVE INGREDIENT SECTION

Aloe Barbadensis Leaf (Aloe Vera Gel) Juice, Aqua (Deionized Water), Camellia Sinensis (Green Tea) Extract, Copper Sulfate, Echinacea Purpurea (Coneflower) Extract, Ethylhexylglycerin, Glycerin, Hydroxyethylcellulose, Lavandula Angustifolia (Lavender) Oil, Mentha Piperita (Peppermint) Oil, Phenoxyethanol, Punica Granatum (Pomegranate) Extract, Sodium Hydroxide, Symphylum Officinale (Comfrey) Extract, Vaccinum Angustifolium (Blueberry) Extract.

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

MiamiBeach1MiamiBeach1MiamiBeach2MiamiBeach2

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
QR code linkQR Codevqr.mx/AX9WUMiamiBeach2.jpg

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
71130-77371130-773-08

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 13 matching rows.

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
0741b4c9-c238-be49-e063-6294a90a17c6441c802f-a35b-1530-e054-00144ff88e882023-10-09WarningsExact identifier
spl set id: 441c802f-a35b-1530-e054-00144ff88e88

Reported adverse events (FAERS/openFDA)#

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