CORALITE PAIN RELIEF- camphor (synthetic), levomenthol and methyl salicylate patch 
United Exchange Corp.

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 Pain Relief Patch 20 Ct

Active ingredients                                     Purpose

DL-Camphor 1.2%.................................. Topical Analgesic

L-Menthol 5.7%...................................... Topical Analgesic

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

Uses

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

Warnings

For external use only

Do not use

Ask a doctor before use if you allergic to any ingredients of this product

When using this product

Stop use and ask a doctor if

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

Caution: This product contains natural rubber latex which may cause allergic reactions

Other information

Inactive ingredients BHT, calcium carbonate, C4-6 olefin/styrene copolymer, glyceryl abiertate, isopropyl myristate, polybutene, polyisobutylene, propylene carbonaterubber latex, sorbitan stearate, ys resin, zinc oxide

DISTRIBUTED BY:

UNITED EXCHANGE CORP.

17211 VALLEY VIEW AVE.

CERRITOS, CA 90703 USA

image description

CORALITE PAIN RELIEF 
dl-camphor, l-menthol, methylsalicylate patch
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:65923-156
Route of Administration TOPICAL DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET) (CAMPHOR (SYNTHETIC) - UNII:5TJD82A1ET) CAMPHOR (SYNTHETIC) 1.2 g  in 100 g
LEVOMENTHOL (UNII: BZ1R15MTK7) (LEVOMENTHOL - UNII:BZ1R15MTK7) LEVOMENTHOL 5.7 g  in 100 g
METHYL SALICYLATE (UNII: LAV5U5022Y) (SALICYLIC ACID - UNII:O414PZ4LPZ) METHYL SALICYLATE 6.3 g  in 100 g
Inactive Ingredients
Ingredient Name Strength
BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)  
CALCIUM CARBONATE (UNII: H0G9379FGK)  
STYRENE (UNII: 44LJ2U959V)  
GLYCERYL ABIETATE (UNII: 2F22LY70Q1)  
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)  
POLYISOBUTYLENE (1000 MW) (UNII: 5XB3A63Y52)  
POLYBUTENE (1400 MW) (UNII: 1NA5AO9GH7)  
PROPYLENE CARBONATE (UNII: 8D08K3S51E)  
ZINC OXIDE (UNII: SOI2LOH54Z)  
Packaging
# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:65923-156-20 20 in 1 PACKAGE
1 1 g in 1 PATCH
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC monograph not final part348 03/26/2014
Labeler - United Exchange Corp. (840130579)

Revised: 3/2014
Document Id: 104a2663-244b-4043-b588-2d33fa611046
Set id: b121c623-d5a8-4ccc-82b1-034e54500560
Version: 1
Effective Time: 20140326
 
United Exchange Corp.