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 88 of 152 · 3,029 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Plantar Fasciitis Cream	CAMPHOR	SOLALIA LLC	388f33c2-2bdf-ded8-e063-6294a90aeeac	2025-06-27	Warnings	Exact identifier application number: M017
4 Lidocaine Topical Anesthetic	LIDOCAINE	RUGBY LABORATORIES	63327e57-f4c8-4ae6-9d28-cef8697bbdcc	2025-06-27	Warnings	Exact identifier application number: M017
Diphenhydramine HCl and Zinc Acetate	ANTI-ITCH CONTINUOUS SPRAY	Wal-Mart Stores, Inc.	709c3bb8-5b36-4823-941a-45ddb3e431c4	2025-06-27	Warnings	Exact identifier application number: M017
Burn Relief Professional Bio-Kool	LIDOCAINE - 4%	Kool-Down Inc.	827e9c69-4706-0ccf-e053-2991aa0aa1c1	2025-06-27	Warnings	Exact identifier application number: M017
Lidocaine Patch	LIDOCAINE	Shenzhen Finona Information Technology Co., Ltd	3875bde5-2e1a-5fdf-e063-6294a90a3c0d	2025-06-26	Warnings	Exact identifier application number: M017
SupreH Bee Venom Arthritis Pain Relieving Cream	SUPREH BEE VENOM ARTHRITIS PAIN RELIEVING CREAM	Shenzhen Xinxin Yunhai Technology Co., Ltd.	3876cc44-7f3a-b084-e063-6294a90a6142	2025-06-26	Warnings	Exact identifier application number: M017
MediBalm	HYDROCORTISONE	BalmRx, LLC	324dd151-84c5-3e2f-e063-6394a90a569d	2025-06-26	Warnings	Exact identifier application number: M017
PHIZICO Pain Relief	MENTHOL	ER3 BRANDS INC.	72715dc5-d1e7-4b4b-8e28-4e367abba322	2025-06-25	Warnings	Exact identifier application number: M017
Diva Cramp Care Cream	METHYL SALICYLATE, MENTHOL, CAMPHOR	Avaria Health & Beauty Corp	37368566-b14e-4d5c-bdde-6eea9073974f	2025-06-25	Warnings	Exact identifier application number: M017
H2Ocean NOTHING TATTOO GLIDE AFTERCARE MAX STRENGTH	LIDOCAINE HCL	H2Ocean, LLC	386bf11b-1d71-44bf-e063-6394a90a2817	2025-06-25	Warnings	Exact identifier application number: M017
Burn Relief Extra Strength Kool-Down	LIDOCAINE - 3.9%	Kool-Down Inc	827fec2f-db3c-adbb-e053-2a91aa0a7c17	2025-06-25	Warnings	Exact identifier application number: M017
Hilook Blue Gel Anesthetic	LIDOCAINE	Guangdong Aimu Biological Technology Co., Ltd	1b9db681-a297-5aa9-e063-6394a90a80ea	2025-06-25	Warnings	Exact identifier application number: M017
Hilook Numbing Cream	LIDOCAINE	Guangdong Aimu Biological Technology Co., Ltd	1b9f1a4c-ca0b-d820-e063-6394a90a3239	2025-06-25	Warnings	Exact identifier application number: M017
Lidocaine Knee Pain Relief Gel-Patch	LIDOCAINE	Guangzhou Zhupuyou E-commerce Co., Ltd	384c1ff8-80bd-86cb-e063-6394a90a2d65	2025-06-24	Warnings	Exact identifier application number: M017
Aroamas Cot Nicotine Transdermal Patches Kit	NICOTINE TRANSDERMAL PATCHES	PCHEERY LLC	38576022-9413-c9af-e063-6294a90afd46	2025-06-24	Warnings	Exact identifier application number: M017
NERVE REVERSE PAIN RELIEF	MENTHOL	Pogue Medical Services	da97bcc6-5aa8-48e2-a2c2-c937745bf6d3	2025-06-23	Warnings	Exact identifier application number: M017
Medterra Pain Relief Menthol Roll-On	MENTHOL	Respect Manufacturing Corporation	05a6067a-287a-52d4-e063-6394a90a2c4e	2025-06-23	Warnings	Exact identifier application number: M017
Medterra Pain Relief 500mg Hemp Menthol Cream	MENTHOL	Respect Manufacturing Corporation	06c4640a-ee42-5d1a-e063-6394a90ad254	2025-06-23	Warnings	Exact identifier application number: M017
Medterra Pain Relief 1000mg Hemp Menthol Cream	MENTHOL	Respect Manufacturing Corporation	06e944e8-71f6-9fe9-e063-6294a90a8c37	2025-06-23	Warnings	Exact identifier application number: M017
Procure gel	MENTHOL	TWIN MED, LLC	e69c0b68-d408-9fd2-e053-2a95a90ac934	2025-06-20	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