DR.SANA ALIVIO TOTAL SPRAY

Manufacturer
EVI LABS
Effective date
2026-03-22
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:51:06

Label at a glance#

ProductDR SANA ALIVIO TOTAL ALIVIO TOTAL
Active ingredientMENTHOL, CAMPHOR (SYNTHETIC)
Label structure13 sections

Indications and uses

Temporarily relieves minor aches and pains of muscles and joints associated with simple backache, arthritis, strains, bruises and sprains.

Dosage and administration

Adults and children 2 years and older: apply to affected areas not more than 3 to 4 times daily. Children under 2 years: ask a doctor.

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Camphor 3 %

Menthol 1.25 %

Purpose

OTC - PURPOSE SECTION

Camphor 3 %.......Topical Analgesic Cream

Menthol 1.25 %.....Topical Analgesic Cream

Uses

INDICATIONS & USAGE SECTION

Temporarily relieves minor aches and pains of muscles and joints associated with simple backache, arthritis, strains, bruises and sprains.

Warnings

WARNINGS SECTION

For external use only. Avoid contact with the eyes.

Flammable: Keep away from excessive heat or open flame.

Do not use

OTC - DO NOT USE SECTION

  • On wounds or damaged skin
  • With a heating pad
  • On a child under 2 years of age with this product

When using this product

OTC - WHEN USING SECTION

  • Avoid contact with eyes or mucous membranes
  • Do not bandage tightly
  • Do not apply to irritated skin

Stop use and ask a doctor if

OTC - STOP USE SECTION

  • Condition worsens
  • Symptoms persist for more than 7 days
  • Symptoms clear up and occur again within a few days
  • Excessive skin irritation occurs

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.

Directions

DOSAGE & ADMINISTRATION SECTION

Adults and children 2 years and older: apply to affected areas not more than 3 to 4 times daily. Children under 2 years: ask a doctor.

Other Information

OTHER SAFETY INFORMATION

Store at 20–25°C (68–77°F). Protect from excessive heat.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water (Aqua), Methyl Salicylate, Glycerin, Cetearyl Alcohol, Mineral Oil (Paraffinum Liquidum), Glyceryl Stearate, Eucalyptus Globulus Leaf Oil, Polysorbate 20, Phenoxyethanol, Xanthan Gum, Disodium EDTA, Tocopheryl Acetate, Arnica Montana Flower Extract, Triethanolamine.

Questions or comments

OTC - QUESTIONS SECTION

Call Weekdays from 9.30 am to 5.00 pm EST at Tel. 305-633-7900

Label Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130729545307053GTIN-13: 0729545307053
EAN-13: 0729545307053
GTIN-12: 729545307053
UPC-A: 729545307053
GTIN storage (14 digits): 00729545307053
Alivio Total Spray 4 oz.jpg

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
84178-109-01DR SANA ALIVIO TOTALALIVIO TOTAL118 g in 1 BOTTLE, PLASTICSPRAY1181

Products#

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

DailyMed product names page 1 of 1 · 17 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
84178-10984178-109-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 15 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
DR SANA ALIVIO TOTAL ALIVIO TOTALALIVIO TOTALEVI LABS4da1c3b8-9af2-6e9f-e063-6394a90a86ae2026-03-22WarningsExact identifier
ndc (package): 84178-109-01
ndc (product): 84178-109
ndc11 (package): 84178010901
spl id: 4da1c3b8-9af3-6e9f-e063-6394a90a86ae
spl set id: 4da1c3b8-9af2-6e9f-e063-6394a90a86ae

Reported adverse events (FAERS/openFDA)#

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