CORALITE COLD AND HOT MEDICATED- menthol 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 Cold & Hot Medicated Patch 1ct Large (90151,2020)

Active ingredient Purpose

Menthol 5%..................................Topical Analgesic

Uses

Warnings

For external use only

Do not use

Ask a doctor before use if you have

When using this product

Stope 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

Other information

Inactive Ingredients alcohol, aluminum glycinate, glycerin, kaolin, methylparaben, polysorbate 80, propylparaben, purified water, sodium polyacrylate, sorbitan monooleate, tartaric acid, titanium dioxide

Questions or comments?

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

Distributed By:

UNITED EXCHANGE CORP.

Cypress, CA. 90630 USA

1-800-814-8028

Made in China

90151

CORALITE COLD AND HOT MEDICATED 
menthol patch
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:65923-154
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL5 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
TARTARIC ACID (UNII: W4888I119H)  
DIHYDROXYALUMINUM AMINOACETATE ANHYDROUS (UNII: 1K713C615K)  
SODIUM POLYACRYLATE (2500000 MW) (UNII: 05I15JNI2J)  
METHYLPARABEN (UNII: A2I8C7HI9T)  
POLYSORBATE 80 (UNII: 6OZP39ZG8H)  
WATER (UNII: 059QF0KO0R)  
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
ALCOHOL (UNII: 3K9958V90M)  
GLYCERIN (UNII: PDC6A3C0OX)  
KAOLIN (UNII: 24H4NWX5CO)  
PROPYLPARABEN (UNII: Z8IX2SC1OH)  
SORBITAN MONOOLEATE (UNII: 06XEA2VD56)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:65923-154-011 in 1 POUCH10/22/2018
15 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 finalpart34810/22/2018
Labeler - United Exchange Corporation (840130579)

Revised: 1/2022
Document Id: d5d1487a-4470-7275-e053-2a95a90a2e7d
Set id: 78da4574-29e8-649f-e053-2991aa0a955d
Version: 4
Effective Time: 20220117
 
United Exchange Corporation