Naturelief

Manufacturer
Novamed Healthcare Private Limited
Effective date
2024-12-16
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 20:45:42

Label at a glance#

ProductNaturelief
Active ingredientGAULTHERIA PROCUMBENS TOP, CAMPHOR (NATURAL), EUCALYPTUS OIL, MENTHOL
Label structure11 sections

Dosage and administration

Apply generously to affected area 3 to 4 time daily Children under 12 consult a doctor before use.

Storage and handling

Store in a cool, dry place between 68 -77 F.

Label contents#

Full prescribing information#

Dosage and Administration

DOSAGE & ADMINISTRATION SECTION

Apply generously to affected area 3 to 4 time daily

Children under 12 consult a doctor before use.

Indication and Usage

INDICATIONS & USAGE SECTION

  • Back pain & Muscle Spasms result due to strain, fatigue & stress
  • USES: Temporarily relieves minor aches & pains related to arthritis, headache, backache, joint and muscle pain, cramps and spasms sprains and other injuries

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Liquid Paraffin, Sodium Lauryl Sulphate, Carbomers BP, Simulgel 600, Sodium Hydroxide

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Wintergreen Oil (Methyl Salicylate) 20%

Eucalyptus Oil 3%

Menthol 2.5%

Camphor 3%

Keep out of the reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of the reach of children

Stop use

OTC - STOP USE SECTION

Stop use and ask a doctor if condition worsens or symptoms persist for more than 7 days

Purpose

OTC - PURPOSE SECTION

Active Ingredient Purpose

Wintergreen Oil (Methyl Salicylate) 20% ...................Topical Analgesic

Eucalyptus Oil 3% ......................................................Anti-Inflammatory

Menthol 2.5% .............................................................Topical Analgesic

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

Storage

STORAGE AND HANDLING SECTION

Store in a cool, dry place between 68 -77 F.

Warning

WARNINGS SECTION

For external use only.

OTC - WHEN USING SECTION

When using this product

  • Discontinue use if excessive irritation of the skin develops.
  • Avoid contact with eyes and mucous membranes.
  • Do not bandage.
  • Do not use with a heating pad.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NatureliefNaturelief

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
84859-11184859-111-25

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 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
3528a453-2b1f-087f-e063-6294a90a9974295de880-4b08-3178-e063-6294a90ab2912025-05-15WarningsExact identifier
spl set id: 295de880-4b08-3178-e063-6294a90ab291

Reported adverse events (FAERS/openFDA)#

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