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 107 of 151 · 3,020 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
DCH Labs Cool and Heat Roll-On	MENTHOL 16%	Derma Care Research Labs, LLC	d35d7720-44ce-3624-e053-2995a90a7fb4	2024-12-19	Warnings	Exact identifier application number: M017
Dr Goldsons Pain	MENTHOL 8%, METHYL SALICYLATE 30%	Derma Care Research Labs, LLC	fb34b0d3-ccc0-305e-e053-6394a90a231d	2024-12-19	Warnings	Exact identifier application number: M017
Warrior Pain Relieving	CAMPHOR 4%, MENTHOL 10%, METHYL SALICYLATE 30%	Derma Care Research Labs, LLC	dd06af3c-5452-9759-e053-2a95a90afc21	2024-12-19	Warnings	Exact identifier application number: M017
Warrior Burn Relief Aloe Maximum Strength	LIDOCAINE HCL 4%	Derma Care Research Labs, LLC	ec6efa4b-dcbe-1c2b-e053-2995a90ae043	2024-12-19	Warnings	Exact identifier application number: M017
DCH Arthritis Relief	TROLAMIN SALICYLATE 10%	Derma Care Research Labs, LLC	ff31e515-5780-b77d-e053-6394a90af6b9	2024-12-19	Warnings	Exact identifier application number: M017
DCH Pain Relief	LIDOCAINE 4%	Derma Care Research Labs, LLC	00efda74-d434-04be-e063-6294a90a6d98	2024-12-19	Warnings	Exact identifier application number: M017
Dollar General Cold Therapy Pain Relief	MENTHOL 5%	Dolgencorp, LLC	ff3284d1-e73c-93bf-e053-6294a90aaf4e	2024-12-19	Warnings	Exact identifier application number: M017
Dollar General Pain Relieving Patch with Lidocaine	LIDOCAINE	DOLGENCORP, LLC	55828cd1-3a1e-48ac-bb01-4c50b96d09a2	2024-12-19	Warnings	Exact identifier application number: M017
DCH Nerve Pain Relief	LIDOCAINE 4%, MENTHOL 1%	Derma Care Research Labs, LLC	00db480a-e510-a64d-e063-6394a90a4695	2024-12-19	Warnings	Exact identifier application number: M017
Pain, Burn, and Itch Relief	BENZOCAINE 20%, MENTHOL 0.5%	Derma Care Research Labs, LLC	fd9fe09f-3ae9-c5f5-e053-6394a90ad691	2024-12-19	Warnings	Exact identifier application number: M017
DCH Cooling Pain Relief	MENTHOL 4%	Derma Care Research Labs, LLC	00ed3175-c3ba-6545-e063-6394a90acfd1	2024-12-19	Warnings	Exact identifier application number: M017
DCH Pain Relief	LIDOCAINE HCL 4%	Derma Care Research Labs, LLC	00dd70f3-ecc3-33ba-e063-6294a90a4f32	2024-12-19	Warnings	Exact identifier application number: M017
Walgreens Kinesiology Pain Relief	LIDOCAINE, MENTHOL	Walgreen Co.	0fdbb310-8e65-4e0c-b413-a093964324a2	2024-12-19	Warnings	Exact identifier application number: M017
Signature Care Medicated Cold and Hot Patch	MENTHOL	Safeway	0335f1b3-5c8a-67b8-e063-6294a90a9847	2024-12-19	Warnings	Exact identifier application number: M017
HealthWise 4% Lidocaine Cream	LIDOCAINE HYDROCHLORIDE	Veridian Healthcare	0fb2af30-7f2d-c7c4-e063-6294a90a37f7	2024-12-19	Warnings	Exact identifier application number: M017
CVS Health Lidocaine Pain Relief	LIDOCAINE HCL	CVS Pharmacy	445b0778-7266-4e72-97cc-e9e0d0066b61	2024-12-18	Warnings	Exact identifier application number: M017
Dr. Scholls Blister Pain Relief Complete	LIDOCAINE	Scholl's Wellness Company LLC	26e3a678-b28f-588b-e063-6394a90ac025	2024-12-18	Warnings	Exact identifier application number: M017
Dr. Scholls Blister Pain Relief Complete	LIDOCAINE	Scholl's Wellness Company LLC	d860b339-48a0-405c-a67d-f7e7a31f6351	2024-12-18	Warnings	Exact identifier application number: M017
TheraCare Pain Relief Lidocaine	LIDOCAINE	Veridian Healthcare	cea6cdab-28a5-5bd0-e053-2a95a90a1295	2024-12-18	Warnings	Exact identifier application number: M017
TheraCare Pain Relief Medicated	LIDOCAINE AND MENTHOL	Veridian Healthcare	0d092461-85fe-acf6-e063-6294a90a5aae	2024-12-18	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