Coralite Blue Ice

Manufacturer
United Exchange Corp.
Effective date
2016-10-05
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:47:26

Label at a glance#

ProductCoralite Blue Ice
Active ingredientMENTHOL
Label structure13 sections

Storage and handling

Other information store in a cool place keep lid tightly closed do not use, pour, spill or store near heat or open flame

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredient                                                   Purpose

Menthol 2%........................................................Topical analgesic   

OTC - PURPOSE SECTION

Uses

  • temporarily relieves minor aches and pains of muscles and joints associated with:
  • arthritis
  • simple backache 
  • strains
  • bruises
  • sport injuries
  • sprains
  • provides cooling penetrating relief

WARNINGS SECTION

Warnings 

For external use only

OTC - DO NOT USE SECTION

Do not use

  • with other topical pain relievers
  • with heating pads or heating devices

OTC - WHEN USING SECTION

When using this product

  • do not use in or near the eyes
  • do not apply to wounds or damaged skin
  • do not bandage tightly

OTC - STOP USE SECTION

Stop use and ask a doctor if

  • condition worsens
  • symptoms last more than 7 days or clear up and occur again within a few days
  • redness or irritation develops

OTC - PREGNANCY OR BREAST FEEDING SECTION

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

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

INDICATIONS & USAGE SECTION

Directions

  • Clean affected area before applying product
  • adults and children 2 years of age and older: apply to affected area not more than 3 to 4 times daily
  • children under 2 years of age: ask a doctor

STORAGE AND HANDLING SECTION

Other information

  • store in a cool place
  • keep lid tightly closed
  • do not use, pour, spill or store near heat or open flame

INACTIVE INGREDIENT SECTION

Inactive ingredients

ammonium hydroxide, carbomer 940, cupric sulfate, FD&C blue no. 1, isopropyl alcohol, magnesium sulfate heptahydrate, purified water, sodium hydroxide, thymol

DOSAGE & ADMINISTRATION SECTION

Distributed by:

United Exchange Corp.

17211 Valley View Ave.

Cerritos, CA 90703 U.S.A.

www.ueccorp.com

Toll Free: 1 800 814 8028

Made in China

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
311502menthol 2 % Topical GelPSN1
311502menthol 0.02 MG/MG Topical GelSCD1
311502menthol 2 % Topical GelSY1
311502menthol 2 % topical stickSY1

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
6e3c022f-0786-43f1-8857-edff89d5153fProduct name120260309
efd58652-cb8f-4018-91ca-4b0eb2ff729fProduct name720240226
6c13b22c-b3ba-4127-b768-0132dd5ab0d1Product name120230829
0306390c-dd77-4363-afe0-63c58088b2a1Product name120220120
503ea967-4b9c-48cf-9e87-c7975295849dProduct name220220120
2641ccb3-721d-4fbf-9f2f-ca2f18157a62Product name320210309
e7e58cd3-cacb-49df-8d34-1ee335614abbProduct name120150609
0ca1d589-929b-4b33-bc5b-1d84abdafa6aProduct name120150324
fc363c46-397b-4476-ac0f-70e43e8e4592Product name120150324

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
65923-157-272020-01-31C16284748780-19d75b9d1-10f5-f424-e053-dadaa90a57ce44ca4bc1-3ee4-420d-9a9a-78b78e6d5c08

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
65923-157-27Coralite Blue Ice227 g in 1 JARGEL2271

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
65923-157CORALITE BLUE ICE (MENTHOL) GEL [UNITED EXCHANGE CORP.]1Legacy NDC, 1 package rows20161011_44ca4bc1-3ee4-420d-9a9a-78b78e6d5c08.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
65923-15765923-157-27

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 10 matching rows.

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
08dcfbb6-eabd-4bb0-ab12-5e59150b72c244ca4bc1-3ee4-420d-9a9a-78b78e6d5c082016-10-05WarningsExact identifier
spl id: 08dcfbb6-eabd-4bb0-ab12-5e59150b72c2
spl set id: 44ca4bc1-3ee4-420d-9a9a-78b78e6d5c08

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.