Green MARVEL ® PAIN RELIEF CREAM

Manufacturer
Miramar Cosmetics, Inc DBA Miramar Lab
Effective date
2026-08-05
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
daily-update
Hydrated at
2026-08-27 00:01:58

Label at a glance#

ProductGreen MARVEL PAIN RELIEF
Active ingredientMENTHOL, UNSPECIFIED FORM, CAMPHOR (NATURAL), METHYL SALICYLATE
Label structure9 sections

Indications and uses

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

Dosage and administration

Adults and children 12 years and older: apply to the affected area not more than 3 to 4 times daily. Children under 12 years: ask a doctor.

Storage and handling

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

Label contents#

Full prescribing information#

Active ingredients (In each 100g) 

OTC - ACTIVE INGREDIENT SECTION

Menthol 4%
Camphor 3%
Methyl salicylate 10%

Purpose

OTC - PURPOSE SECTION

Topical analgesic

Uses

INDICATIONS & USAGE SECTION

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

Warnings

WARNINGS SECTION

For external use only

Allergy alert: Contains salicylate.

Do not use: On wounds or damaged skin. On irritated skin. With a heating pad.

Ask a doctor before use if you have: Allergies to salicylates.

When using this product
Avoid contact with eyes and mucous membranes. Do not bandage tightly.

Stop use and ask a doctor if
Condition worsens. Symptoms persist for more than 7 days. Irritation develops. If pregnant or breast-feeding, ask a health professional before use.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.
If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

Adults and children 12 years and older: apply to the affected area not more than 3 to 4 times daily. Children under 12 years: ask a doctor.

Other information

STORAGE AND HANDLING SECTION

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

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water (Aqua), Glycerin, Xanthan Gum, Hydrogenated Castor Oil, Triethanolamine, Carbomer, Arnica Oil, Cannabis Sativa Seed Oil, Aloe Barbadensis Leaf, Chamomilla Recutita (Matricaria) Flower Extract, Oryza Sativa (Rice) Extract, Calendula Officinalis Flower Extract, Melissa Oil, Eucalyptus Globulus Oil, FD&C Blue No. 1, FD&C Yellow No. 5, Methylisothiazolinone.

SPL UNCLASSIFIED SECTION

NATURE MADE SCIENCE
WITH NATURAL INGREDIENTS

Carthamus Tinctorius
Chamomile
Cilantro
Gaultheria procumbens
Hamamelis Virginiana
Linden
Willow Bark

Distributed by: Prestige Brands LLC, Multichannel Retail & Logistics,
145 Union St. Unit O Holbrook, MA 02343
Questions or comments. Call toll-free: 1-800-508-9784

Manufactured in USA

GOOD MANUFACTURING PRACTICE

GMP CERTIFIED

• Fresh sensation
• Fast absorption
• Non-greasy
• Does not stain clothes

Paraben-Free 
Gluten-Free
Cruelty-Free

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

GreenMarvelPainReliefGreenMarvelPainRelief

Products#

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

DailyMed product names page 1 of 1 · 24 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
79974-22079974-220-04

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 20 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
Green MARVEL PAIN RELIEFMENTHOL, CAMPHOR, METHYL SALICYLATEMiramar Cosmetics, Inc DBA Miramar Lab9ff6e477-ef79-4a0c-9e21-8cae0e5d88102026-08-05WarningsExact identifier
ndc (package): 79974-220-04
ndc (product): 79974-220
ndc11 (package): 79974022004
spl id: bf9f0058-29d7-4b33-a9c0-ef830b67c421
spl set id: 9ff6e477-ef79-4a0c-9e21-8cae0e5d8810

Reported adverse events (FAERS/openFDA)#

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