DR. LUKE ARNICA BRUISE CREAM- arnica bruise cream cream

Dr. Luke Arnica Bruise Cream by

Drug Labeling and Warnings

Dr. Luke Arnica Bruise Cream by is a Otc medication manufactured, distributed, or labeled by DANOUS LAND FLOOW LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Arnica Montana 1x HPUS

PURPOSE

Reduces pain, swelling, and discoloration from bruises

WHEN USING

Avoid contact with eyes, mucous membranes. If contact occurs, rinse with water.
Use only as directed
Do not tightly wrap or bandage the treated area.
Do not apply heat or ice to the treated area immediately.

DO NOT USE

Do not apply to open wounds or broken skin.
You are allergic to arnica montana, or other inactive ingredients in this product

KEEP OUT OF REACH OF CHILDREN

If swallowed, get medical help or contact a Poison Control Center right away.

WARNINGS

For external use only.

INACTIVE INGREDIENT

Water, Glycerin, Cocos Nucifera (Coconut) Oil, Grape Seed Oil,Dimethicone, Beeswax, Acrylates Crosspolymer-6, Niacinamide, Hippophae
Rhamnoides Fruit Oil, Trehalose, Propylene Glycol, Phytonadione (Vitamin
K1), Hydroxyethylcellulose, Polyacrylamide, Vitamin E, Vitamin C, Lavender
Oil, Rosemary Leaf Oil, Boswellia Carterii (Frankincense) Oil, Panax
Notoginseng Root Extract, Liposomal Curcumin, Laureth-7, 1,2-Hexanediol,
pH Adjusters, Ethylhexylglycerin, Polysorbate 60.

INSTRUCTIONS FOR USE

Apply a thin layer of bruise cream to affected areas 3 times daily.
Massage gently until fully absorbed.
For best results, use consistently until appearance improves.

INDICATIONS & USAGE

Reduces symptoms of bruising such as: Pain, Swelling, Discoloration

DOSAGE & ADMINISTRATION

Apply to affected area not more than 3–4 times daily.

OTHER SAFETY INFORMATION

Do not use if glued carton end flaps are open or if the tube seal is broken.
Store at 68°-77°F (20°-25C).
Keep container tightly closed

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

DR. LUKE ARNICA BRUISE CREAM 
arnica bruise cream cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 87147-004
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ARNICA MONTANA WHOLE (UNII: O80TY208ZW) (ARNICA MONTANA WHOLE - UNII:O80TY208ZW)	ARNICA MONTANA WHOLE	5 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
ALPHA-TOCOPHEROL (UNII: H4N855PNZ1)
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
COCOS NUCIFERA (COCONUT) OIL (UNII: Q9L0O73W7L)
GRAPE SEED OIL (UNII: 930MLC8XGG)
DIMETHICONE (UNII: 92RU3N3Y1O)
BEESWAX (UNII: 2ZA36H0S2V)
NIACINAMIDE (UNII: 25X51I8RD4)
HIPPOPHAE RHAMNOIDES FRUIT OIL (UNII: TA4JCF9S1J)
TREHALOSE (UNII: B8WCK70T7I)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
PHYTONADIONE (UNII: A034SE7857)
LAVENDER OIL (UNII: ZBP1YXW0H8)
HYDROXYETHYLCELLULOSE (UNII: T4V6TWG28D)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 87147-004-01	114 g in 1 JAR; Type 0: Not a Combination Product	10/13/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M017	10/13/2025

Labeler - DANOUS LAND FLOOW LLC (067045402)