FDA.reportPublic FDA data

Coralite Ultra Strength Pain Relief

Product NDC
65923-532
11-digit product format
659230532
Labeler code
65923
Product ID
65923-532_425530d6-e8ea-f05c-e063-6294a90aff39
Type
HUMAN OTC DRUG
Nonproprietary name
Camphor Menthol
Dosage form
OINTMENT
Route
TOPICAL
Labeler
United Exchange Corp.
Application
M017
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2014-10-15
Substance
CAMPHOR (SYNTHETIC); MENTHOL
Active strength
110; 110 mg/g; mg/g
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Coralite Ultra Strength Pain Relief
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
CAMPHOR (SYNTHETIC)110 mg/g
MENTHOL110 mg/g

Harmonized Identifiers#

Field, Values table
FieldValues
Unii5TJD82A1ET, L7T10EIP3A
Rxcui1089831

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
65923-532-182022-03-31C16284748780-1d6a99b39-7496-a426-e053-dadaa90af4c2Coralite Ultra Strength Pain Relief Balm 0.63oz (532)
65923-532-182022-03-31C16284748780-1d6a99b39-7496-a426-e053-dadaa90af4c2Coralite Ultra Strength Pain Relief Balm 0.63oz (532)
65923-532-182022-01-28C16284748780-1d6a99b39-7496-a426-e053-dadaa90af4c2Coralite Ultra Strength Pain Relief Balm 0.63oz (532)
65923-532-182022-01-28C16284748780-1d6a99b39-7496-a426-e053-dadaa90af4c2Coralite Ultra Strength Pain Relief Balm 0.63oz (532)

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
65923-532-18Coralite Ultra Strength Pain Relief1 in 1 CARTONOINTMENT113
65923-532-18Coralite Ultra Strength Pain Relief18 g in 1 JAROINTMENT1813

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
CAMPHOR (SYNTHETIC)ACTIVE INGREDIENT5TJD82A1ETCORALITE ULTRA STRENGTH PAIN RELIEF (CAMPHOR MENTHOL) OINTMENT [UNITED EXCHANGE CORP.]1
MENTHOLACTIVE INGREDIENTL7T10EIP3ACORALITE ULTRA STRENGTH PAIN RELIEF (CAMPHOR MENTHOL) OINTMENT [UNITED EXCHANGE CORP.]1
CAMPHOR (SYNTHETIC)ACTIVE MOIETY5TJD82A1ETCORALITE ULTRA STRENGTH PAIN RELIEF (CAMPHOR MENTHOL) OINTMENT [UNITED EXCHANGE CORP.]1
MENTHOLACTIVE MOIETYL7T10EIP3ACORALITE ULTRA STRENGTH PAIN RELIEF (CAMPHOR MENTHOL) OINTMENT [UNITED EXCHANGE CORP.]1
CAJUPUT OILINACTIVE INGREDIENTJ3TO6BUQ37CORALITE ULTRA STRENGTH PAIN RELIEF (CAMPHOR MENTHOL) OINTMENT [UNITED EXCHANGE CORP.]1
CLOVE OILINACTIVE INGREDIENT578389D6D0CORALITE ULTRA STRENGTH PAIN RELIEF (CAMPHOR MENTHOL) OINTMENT [UNITED EXCHANGE CORP.]1
PARAFFININACTIVE INGREDIENTI9O0E3H2ZECORALITE ULTRA STRENGTH PAIN RELIEF (CAMPHOR MENTHOL) OINTMENT [UNITED EXCHANGE CORP.]1
PETROLATUMINACTIVE INGREDIENT4T6H12BN9UCORALITE ULTRA STRENGTH PAIN RELIEF (CAMPHOR MENTHOL) OINTMENT [UNITED EXCHANGE CORP.]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
65923-532CORALITE ULTRA STRENGTH PAIN RELIEF (CAMPHOR MENTHOL) OINTMENT [UNITED EXCHANGE CORP.]11Current NDC, Legacy NDC, 2 package rows20241222_44ecf959-cc07-4adc-a500-075b2ee69548.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
1089831camphor 11 % / menthol 11 % Topical CreamPSN44ecf959-cc07-4adc-a500-075b2ee6954813
1089831camphor 110 MG/ML / menthol 110 MG/ML Topical CreamSCD44ecf959-cc07-4adc-a500-075b2ee6954813
1089831camphor 11 % / menthol 11 % Topical CreamSY44ecf959-cc07-4adc-a500-075b2ee6954813

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
65923-532-18659230532181 JAR in 1 CARTON (65923-532-18) / 18 g in 1 JAR1 jar2017-12-130000-00-00NoNoCurrent