CORALITE MUSCLE AND JOINT PAIN RELIEF- camphor, menthol, and mehtyl salicylate patch 
United Exchange Corporation

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Coralite Muscle & Joint Pain Relief patch 2ct (90155)

Active Ingredients Purposes

Camphor 1.2%...................Topical analgesic

Menthol 5.7%.....................Topical analgesic

Methyl salicylate 6.3%.......Topical analgesic

Uses

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 contact a Poison Control Center (1-800-222-1222) right away.

Directions

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

Call 1-800-814-8028 Monday-Friday 9AM-5PM (PST)

Distributed By:

UNITED EXCHANGE CORP.

Cypress, CA. 90630 USA

Made in China

90155

CORALITE MUSCLE AND JOINT PAIN RELIEF 
camphor, menthol, and mehtyl salicylate patch
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:65923-148
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET) (CAMPHOR (SYNTHETIC) - UNII:5TJD82A1ET) CAMPHOR (SYNTHETIC)12 mg  in 1 g
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL57 mg  in 1 g
METHYL SALICYLATE (UNII: LAV5U5022Y) (SALICYLIC ACID - UNII:O414PZ4LPZ) METHYL SALICYLATE63 mg  in 1 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)  
POLYISOBUTYLENE (800000 MW) (UNII: Y132ZOQ9H7)  
POLYISOBUTYLENE (85000 MW) (UNII: 7X53O5S2ZY)  
STYRENE/ISOPRENE/STYRENE BLOCK COPOLYMER (STYRENE/ISOPRENE 15/85) (UNII: 1SSZ6HXE7P)  
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
ZINC OXIDE (UNII: SOI2LOH54Z)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:65923-148-021 in 1 POUCH10/23/2018
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 not finalpart34810/23/2018
Labeler - United Exchange Corporation (840130579)

Revised: 6/2023
Document Id: fda5459f-9f62-1a9f-e053-6394a90a1747
Set id: 78edeeb8-3e3c-64bb-e053-2a91aa0a7bbc
Version: 7
Effective Time: 20230608
 
United Exchange Corporation