CORALITE PAIN RELIEF- dl-camphor, l-menthol, methylsalicylate 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 Patch 40 ct. 90156 (2018)

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:

arthritis
simple backache
strains
bruises
sprains

Warnings

For external use only

Do not use

on wounds or damaged skin
if you are allergic to aspirin or salicylates
with a heating pad
with, or at the same time as, other external analgesic products

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

When using this product

do not use other than directed
avoid contact with the eyes, mucous membranes or rashes

Stop use and ask a doctor if

rash, itching or excessive skin irritation develops
conditions worsen symptoms persist for more than 7 days
symptoms clear up and occur again within a few days

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

avoid storing product in direct sunlight
protect from excessive moisture

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

90156

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

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
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

Ingredient Name	Strength
Inactive Ingredients
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)

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:65923-156-20	20 in 1 PACKAGE	04/18/2016
1		1 g in 1 PATCH; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph not final	part348	03/26/2014	01/01/2018

Labeler - United Exchange Corp. (840130579)

Revised: 4/2018

Document Id: 69c46cef-9b1c-1ab9-e053-2a91aa0ac2e3

Set id: b121c623-d5a8-4ccc-82b1-034e54500560

Version: 7

Effective Time: 20180413

United Exchange Corp.