Magnilife Knee pain relief gel

Magnilife Knee pain relief gel by

Drug Labeling and Warnings

Magnilife Knee pain relief gel by is a Homeopathic medication manufactured, distributed, or labeled by United Laboratories Manufacturing, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

MAGNILIFE KNEE PAIN RELIEF GEL- arnica montana flower, toxicodendron pubescens leaf gel 
United Laboratories Manufacturing, LLC

Disclaimer: This homeopathic product has not been evaluated by the Food and Drug Administration for safety or efficacy. FDA is not aware of scientific evidence to support homeopathy as effective.

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Magnilife Knee pain relief gel

Drug Facts

Active ingredients (in gel)

Arnica 1X

Rhus Tox 4X

Purpose

Pain reliever

For joint pain

Uses

Temporary relief from minor aches and pains of sore muscles and joints associated with: Arthritis Knee Pain Strains Sprains

Warnings

For external use only 

Keep out of reach of children

Stop use and ask a doctor

if you experience worsening symptoms or if symptoms last longer than 7 days Avoid contact with the eyes or mucous membranes Do not apply to wounds or damaged skin  Wash hands after use

If pregnant or breastfeeding,

ask a health professional before use

Directions

Adults and children 12 years and older, generously apply and massage into affected areas.

Other information

*These statements are based upon traditional homeopathic practice. They have not been reviewed by the Food and Drug Administration.

Inactive ingredients

Alcohol, Aloe Barbadensis Leaf Extract, Benzoic Acid, Carbomer, Croton Lechleri Resin Extract, Dimethyl Sulfone, Glycerin, Hamamelis Virginiana (Witch Hazel) Water, Menthyl Nicotinate, Phenoxyethanol, Sorbic Acid, Tromethamine, Uncaria Tomentosa Extract, Water (Aqua)

Package Labeling:

MAGNILIFE KNEE PAIN RELIEF GEL 
arnica montana flower, toxicodendron pubescens leaf gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 62400-0055
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ) (ARNICA MONTANA FLOWER - UNII:OZ0E5Y15PZ)	ARNICA MONTANA FLOWER	1 [hp_X]  in 1 g
TOXICODENDRON PUBESCENS LEAF (UNII: 6IO182RP7A) (TOXICODENDRON PUBESCENS LEAF - UNII:6IO182RP7A)	TOXICODENDRON PUBESCENS LEAF	4 [hp_X]  in 1 g

Inactive Ingredients
Ingredient Name	Strength
ALCOHOL (UNII: 3K9958V90M)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
BENZOIC ACID (UNII: 8SKN0B0MIM)
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
CROTON LECHLERI RESIN (UNII: GGG6W25C63)
DIMETHYL SULFONE (UNII: 9H4PO4Z4FT)
GLYCERIN (UNII: PDC6A3C0OX)
HAMAMELIS VIRGINIANA TOP WATER (UNII: NT00Y05A2V)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
SORBIC ACID (UNII: X045WJ989B)
TROMETHAMINE (UNII: 023C2WHX2V)
CAT'S CLAW (UNII: 9060PRM18Q)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 62400-0055-1	113 g in 1 JAR; Type 0: Not a Combination Product	02/10/2022	09/04/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved homeopathic		02/10/2022	09/04/2025

Labeler - United Laboratories Manufacturing, LLC (807878116)

Establishment
Name	Address	ID/FEI	Business Operations
United Laboratories Manufacturing, LLC		807878116	manufacture(62400-0055) , label(62400-0055) , pack(62400-0055)

Revised: 9/2025

Document Id: 3f01a409-a521-bddc-e063-6394a90a3011

34390-5

Set id: d825893d-e902-75d9-e053-2a95a90a477f

Version: 2

Effective Time: 20250917