UNIVERSAL ARTHRITIS AND SPORT- methyl salicylate, capsicum liquid

Universal ARTHRITIS and SPORT by

Drug Labeling and Warnings

Universal ARTHRITIS and SPORT by is a Otc medication manufactured, distributed, or labeled by Universal Distribution Center LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active ingredients

Methyl Salicylate 0.61%

Capsicum 0.0012%

Purpose

Topical Analgesic

Uses

for the temporary relief of minor aches and pains of muscles and joints associated with:

simple backache  arthritis strains bruises sprains

Warnings

For external use only

Do not use other than as directed on children under 12 years of age

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

Directions

Adults and children 12 years of age and older: apply to affected area not more than 3 to 4 times daily

Children under 12 years of age: ask a doctor

Inactive ingredients

FD&C Blue No.1 (CI 42090), Isopropyl Alcohol, Magnesium Sulfate, Menthol, Water (Aqua)

SPL UNCLASSIFIED SECTION

COOL BLUE ICE

Formulated for:

Rubbing and Soaking

Arthritis Aching Stiff Joints
Aching Muscles Tired Aching Feet Sprains

Extra Strength 

with Rubbing Alcohol

Distributed by:
Universal Distribution Center LLC.
96 Distribution Boulevard, Edison,
NJ 08817

www.universaldc.com

Made in Jordan

Packaging

INGREDIENTS AND APPEARANCE

UNIVERSAL ARTHRITIS AND SPORT 
methyl salicylate, capsicum liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 52000-302
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
METHYL SALICYLATE (UNII: LAV5U5022Y) (SALICYLIC ACID - UNII:O414PZ4LPZ)	METHYL SALICYLATE	0.61 g  in 100 mL
CAPSICUM (UNII: 00UK7646FG) (CAPSICUM - UNII:00UK7646FG)	CAPSICUM	0.0012 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
ISOPROPYL ALCOHOL (UNII: ND2M416302)
MAGNESIUM SULFATE, UNSPECIFIED FORM (UNII: DE08037SAB)
MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A)
WATER (UNII: 059QF0KO0R)

Product Characteristics
Color	blue	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 52000-302-33	473 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	11/01/2023

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M017	11/01/2023

Labeler - Universal Distribution Center LLC (019180459)