Melt Pain Away

Manufacturer
NATURLAND Magyarorszag Termelo es Kereskedelmi Korlatolt Felelossegu Tarsasag
Effective date
2024-08-13
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 20:56:46

Label at a glance#

ProductMelt Pain Away
Active ingredientCAPSAICIN
Label structure9 sections

Storage and handling

Store in a cool, dry place. Keep away from excessive heat or flame. Tamper-evident for your protection. Use only if safety seal is intact

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Capsaicin .025%

OTC - PURPOSE SECTION

Topical Analgesic

INDICATIONS & USAGE SECTION

Temporarily relieves minor aches and pains of muscles and joints associated with:

  • arthritis
  • simple backache
  • strains
  • sprains
  • bruises

WARNINGS SECTION

Use only as directed.

For external use only.

OTC - WHEN USING SECTION

When using this product:

  • avoid contact with eyes
  • do not apply to wounds or damaged skin
  • do not bandage tightly

OTC - STOP USE SECTION

Stop use and ask doctor if:

  • condition worsens
  • symptoms persist for more than 7 days, or clear up and reoccur again with a few days
  • redness is present
  • irritation develops.

OTC - PREGNANCY OR BREAST FEEDING SECTION

If pregnant or breastfeeding,ask a health professional before use.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If accidentally ingested, get medical help or contact Poison Control Center immediately.

DOSAGE & ADMINISTRATION SECTION

Adults and children over 18 years:

  • Apply to affected area. Massage into the painful area until thoroughly absorbed. Repeat as necessary but no more than 3 to 4

times daily.

  • Wash hands with soap and water after applying.

Children 18 years and younger:

  • Consult a doctor.

STORAGE AND HANDLING SECTION

  • Store in a cool, dry place.
  • Keep away from excessive heat or flame.
  • Tamper-evident for your protection. Use only if safety seal is intact

INACTIVE INGREDIENT SECTION

Water, Magnesium Chloride, Prunus Amygdalus Dulcis (Sweet Almond) Oil, Cetearyl Alcohol, Butyrospermum Parkii (Shea) Butter, Dimethyl Sulfone (MSM), Sodium Lactate, Glyceryl Stearate Citrate, Cetyl Palmitate, Glycerin, Glyceryl Stearate, Polyglyceryl-3 Diisostearate, Pentylene Glycol, Undecane, Xanthan Gum, Magnesium Sulfate, Tridecane, Potassium Chloride, Sodium Chloride, Calcium Chloride, Tocopheryl Acetate (Vitamin E), Hydroxyacetophenone, Panthenol, Allantoin, Pentaerythrityl Tetra-Di-T-Butyl Hydroxyhydrocinnamate, Sodium Hydroxide, Cymbopogon Flexuosus (East-Indian Lemongrass) Oil* *Organic

OTC - QUESTIONS SECTION

888-819-6472; Monday–Friday, 9am–5pm CT
Report any serious side effects to number above.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Melt Pain AwayMelt Pain Away

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
84618-003MELT PAIN AWAY (CAPSAICIN) CREAM [NATURLAND MAGYARORSZAG TERMELO ES KERESKEDELMI KORLATOLT FELELOSSEGU TARSASAG]1Unmatched20240815_1f91cb05-dae7-8075-e063-6394a90ae7a2.zip

Products#

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

DailyMed product names page 1 of 1 · 29 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
84618-00384618-003-01, 84618-003-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 28 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
37da3e2a-3a3c-1784-e063-6394a90a969f1f91cb05-dae7-8075-e063-6394a90ae7a22025-06-18WarningsExact identifier
spl set id: 1f91cb05-dae7-8075-e063-6394a90ae7a2

Reported adverse events (FAERS/openFDA)#

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