CORALITE PAIN RELIEF- camphor, menthol, methyl salicylate patch 
United Exchange Corp.

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Coralite Small Pain Relief Patch 20 ct. 90156

Active ingredients Purpose

Camphor 1.2%........................................Topical Analgesic

Menthol 5.7%..........................................Topical Analgesic

Methyl Salicylate 6.3%............................Topical Analgesic

Uses

For temporary relief of minor aches & pains of muscles & joints associated with:

Warnings

For external use only

Allergy alert: If prone to allergic reaction from aspirin or salicylates, consult a doctor before use.

Do not use

Ask a doctor before use if you have redness over the affected area.

When using this product

Stop use and ask a doctor if

If pregnant or breast-feeding, ask a health professional before use.

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

Directions

adults and children 12 years of age and over:

Other information

Inactive ingredients

aluminum silicate, butylated hydroxytoluene, glyceryl rosinate, lanolin, natural rubber, paraffin, polyisobutylene (800000 mw), polyisobutylene (85000 mw), styrene-isoprene-styrene block copolymer, titanium dioxide, zinc oxide

Distributed by:

United Exchange Corp.

Cypress, CA 90630 USA

Made in China

90156

CORALITE PAIN RELIEF 
camphor, menthol, methyl salicylate patch
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:65923-564
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET) (CAMPHOR (SYNTHETIC) - UNII:5TJD82A1ET) CAMPHOR (SYNTHETIC)1.2 g  in 100 g
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL5.7 g  in 100 g
METHYL SALICYLATE (UNII: LAV5U5022Y) (SALICYLIC ACID - UNII:O414PZ4LPZ) METHYL SALICYLATE6.3 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
ALUMINUM SILICATE (UNII: T1FAD4SS2M)  
BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)  
GLYCERYL ROSINATE (UNII: SD112V492J)  
LANOLIN (UNII: 7EV65EAW6H)  
NATURAL LATEX RUBBER (UNII: 2LQ0UUW8IN)  
PARAFFIN (UNII: I9O0E3H2ZE)  
STYRENE/ISOPRENE/STYRENE BLOCK COPOLYMER (UNII: K7S96QM8DV)  
POLYISOBUTYLENE (85000 MW) (UNII: 7X53O5S2ZY)  
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
POLYISOBUTYLENE (800000 MW) (UNII: Y132ZOQ9H7)  
ZINC OXIDE (UNII: SOI2LOH54Z)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:65923-564-2020 in 1 PACKAGE04/12/2018
11 g in 1 PATCH; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01704/12/2016
Labeler - United Exchange Corp. (840130579)

Revised: 10/2025
Document Id: 41b49d77-4471-c6ae-e063-6394a90aaac6
Set id: 69aec845-3d4c-d226-e053-2991aa0afd12
Version: 10
Effective Time: 20251021
 
United Exchange Corp.