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

Reported adverse events (FAERS/openFDA)#

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

Additional Listing Data#

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

Active Ingredients#

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

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 2 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
5TJD82A1ET	Internal UNII lookup
L7T10EIP3A	Internal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
1089831	Internal RxNorm lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
44ecf959-cc07-4adc-a500-075b2ee69548	Available on FDA.report

FDA-Initiated Inactive NDC Indexing#

Effective, Related label table
Effective	Related label
2022-03-31	Coralite Ultra Strength Pain Relief Balm 0.63oz (532)
2022-03-31	Coralite Ultra Strength Pain Relief Balm 0.63oz (532)
2022-01-28	Coralite Ultra Strength Pain Relief Balm 0.63oz (532)
2022-01-28	Coralite Ultra Strength Pain Relief Balm 0.63oz (532)

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
65923-532-18	Coralite Ultra Strength Pain Relief	1 in 1 CARTON	OINTMENT	1		13
65923-532-18	Coralite Ultra Strength Pain Relief	18 g in 1 JAR	OINTMENT	18		13

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
CAMPHOR (SYNTHETIC)	ACTIVE INGREDIENT	5TJD82A1ET	CORALITE ULTRA STRENGTH PAIN RELIEF (CAMPHOR MENTHOL) OINTMENT [UNITED EXCHANGE CORP.]	1
MENTHOL	ACTIVE INGREDIENT	L7T10EIP3A	CORALITE ULTRA STRENGTH PAIN RELIEF (CAMPHOR MENTHOL) OINTMENT [UNITED EXCHANGE CORP.]	1
CAMPHOR (SYNTHETIC)	ACTIVE MOIETY	5TJD82A1ET	CORALITE ULTRA STRENGTH PAIN RELIEF (CAMPHOR MENTHOL) OINTMENT [UNITED EXCHANGE CORP.]	1
MENTHOL	ACTIVE MOIETY	L7T10EIP3A	CORALITE ULTRA STRENGTH PAIN RELIEF (CAMPHOR MENTHOL) OINTMENT [UNITED EXCHANGE CORP.]	1
CAJUPUT OIL	INACTIVE INGREDIENT	J3TO6BUQ37	CORALITE ULTRA STRENGTH PAIN RELIEF (CAMPHOR MENTHOL) OINTMENT [UNITED EXCHANGE CORP.]	1
CLOVE OIL	INACTIVE INGREDIENT	578389D6D0	CORALITE ULTRA STRENGTH PAIN RELIEF (CAMPHOR MENTHOL) OINTMENT [UNITED EXCHANGE CORP.]	1
PARAFFIN	INACTIVE INGREDIENT	I9O0E3H2ZE	CORALITE ULTRA STRENGTH PAIN RELIEF (CAMPHOR MENTHOL) OINTMENT [UNITED EXCHANGE CORP.]	1
PETROLATUM	INACTIVE INGREDIENT	4T6H12BN9U	CORALITE ULTRA STRENGTH PAIN RELIEF (CAMPHOR MENTHOL) OINTMENT [UNITED EXCHANGE CORP.]	1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
65923-532	CORALITE ULTRA STRENGTH PAIN RELIEF (CAMPHOR MENTHOL) OINTMENT [UNITED EXCHANGE CORP.]	11	Current NDC, Legacy NDC, 2 package rows	20241222_44ecf959-cc07-4adc-a500-075b2ee69548.zip

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 80 of 152 · 3,029 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
HealthWise Overnight Menthol Patch	MENTHOL	Veridian Healthcare	6379f50d-2878-46ca-8acb-71c4554585e9	2025-08-28	Warnings	Exact identifier application number: M017
Anti Itch Maximum Relief	PRAMOXINE HYDROCHLORIDE AND MENTHOL	Natureplex LLC	75de3d5e-ecbe-4d04-a39d-792200e6ee32	2025-08-28	Warnings	Exact identifier application number: M017
NicDuic Quit Smoking Nicotine Patches	NICOTINE TRANSDERMAL PATCHES	Shenzhen Paxi Trading Co., Ltd.	3d5718f3-c175-6b64-e063-6394a90aa6f1	2025-08-27	Warnings	Exact identifier application number: M017
ARCTIC HEAT	MENTHOL, METHYL SALICYLATE	Renu Laboratories, LLC	402df5c1-b8cb-17a2-e054-00144ff8d46c	2025-08-27	Warnings	Exact identifier application number: M017
PROHEAL HYDROCORTISONE 1% MAXIMUM STRENGTH PLUS ALOE	HYDROCORTISONE	Click Industries LLC	328c389c-7e05-4892-a9b3-b6a753f4935a	2025-08-25	Warnings	Exact identifier application number: M017
Yeheal	CAMPHOR, MENTHOL, ISOPROPYL ALCOHOL	Shenzhen Yeheal Biotechnology Co., Ltd	3cf1bc74-3060-6d63-e063-6294a90a9f5c	2025-08-22	Warnings	Exact identifier application number: M017
Dermedial Anti-Ouch	MENTHOL	Natures Formulae Health Products Ltd.	3ce29160-3964-e435-e063-6394a90abb38	2025-08-21	Warnings	Exact identifier application number: M017
SUGARLOAF ORGANICS MENTHOL REVIVE	MENTHOL	RENU LABORATORIES, LLC	fa2f9539-b703-a00b-e053-6394a90ae309	2025-08-21	Warnings	Exact identifier application number: M017
Camphor 4% Plus Menthol 10%	CAMPHOR 4% PLUS MENTHOL 10%	PureTek Corporation	3cab26e4-e377-f26a-e063-6394a90a17af	2025-08-20	Warnings	Exact identifier application number: M017
Capsaicin 0.035% Cream	CAPSAICIN 0.035% CREAM	Puretekcorp	3cbc73b6-8c58-8f23-e063-6394a90a71a3	2025-08-20	Warnings	Exact identifier application number: M017
Game On	MENTHOL, METHYL SALICYLATE	Natural Essentials, Inc.	3cd20f1f-033f-f698-e063-6294a90a89eb	2025-08-20	Warnings	Exact identifier application number: M017
ELAIMEI Numbing Cream	LIDOCAINE 4%	Shenzhen Shandian Jingling Technology Co., Ltd.	37ac13b2-ca55-0e28-e063-6294a90a000e	2025-08-19	Warnings	Exact identifier application number: M017
Calamine Plus Pramoxine HCl	CALAMINE PLUS SPRAY	FSA Store Inc.	3cd18f96-34f7-3f2c-e063-6294a90a3b7e	2025-08-19	Warnings	Exact identifier application number: M017
Hydrocortisone	HYDROCORTISONE SPRAY	FSA Store Inc.	3ce24b87-55ac-0bbd-e063-6294a90ab582	2025-08-19	Warnings	Exact identifier application number: M017
Fast Freeze Pain Relieving	MENTHOL, UNSPECIFIED FORM	NATURAL ESSENTIALS, INC.	15a26af1-ca5a-40fc-a411-6c0e8ae18fbb	2025-08-18	Warnings	Exact identifier application number: M017
Orythia Maximum Strength Lidocaine Pain Relieving	LIDOCAINE	Planet (Anhui) Pharmaceutical Co., Ltd.	6d6b59f9-f614-4e3c-b07b-32b4591d39f2	2025-08-18	Warnings	Exact identifier application number: M017
Ocean Potion Suncare Ice Plus Pain Relieving Soothing	LIDOCAINE	GNL BRANDS INTERNATIONAL, LLC	3c69654c-cba6-dfef-e063-6394a90ad479	2025-08-15	Warnings	Exact identifier application number: M017
Earth Mama Medicated Herbal Lip Balm	MENTHOL	Eleeo Brands LLC	3c6c16bb-1f4b-b851-e063-6294a90a7404	2025-08-15	Warnings	Exact identifier application number: M017
Lidocaine Hydrochloride	LIDOCAINE HYDROCHLORIDE	Cintas First Aid & Safety	96f17095-31f3-4b8a-ab22-0caaefaa7476	2025-08-15	Warnings	Exact identifier application number: M017
MedPride Cold Ice Analgesic Gel	MENTHOL	SHIELD LINE LLC	860a2c86-b240-4e0e-e053-2a91aa0a333a	2025-08-15	Warnings	Exact identifier application number: M017

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
5TJD82A1ET	CAMPHOR (SYNTHETIC)	76-22-2	CAMPHOR (SYNTHETIC)

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
1089831	camphor 11 % / menthol 11 % Topical Cream	PSN	44ecf959-cc07-4adc-a500-075b2ee69548	13
1089831	camphor 110 MG/ML / menthol 110 MG/ML Topical Cream	SCD	44ecf959-cc07-4adc-a500-075b2ee69548	13
1089831	camphor 11 % / menthol 11 % Topical Cream	SY	44ecf959-cc07-4adc-a500-075b2ee69548	13

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
65923-532-18	65923053218	1 JAR in 1 CARTON (65923-532-18) / 18 g in 1 JAR	1 jar	2017-12-13	0000-00-00	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
Coralite Ultra Strength Pain Relief Balm 0.63oz (532)	United Exchange Corp.	2025-10-29	HUMAN OTC DRUG LABEL	13