Ultra strength pain relief balm

Product NDC: 76168-331
Requested package NDC: 76168-331-18
11-digit product format: 761680331
Labeler code: 76168
Product ID: 76168-331_edf30b05-987d-b701-e053-2a95a90a9849
Type: HUMAN OTC DRUG
Nonproprietary name: Camphor (Synthetic) and Menthol
Dosage form: OINTMENT
Route: TOPICAL
Labeler: Velocity Pharma LLC
Application: part348
Marketing category: OTC MONOGRAPH NOT FINAL
Marketing start: 2020-09-10
Marketing end: 0000-00-00
Substance: CAMPHOR (SYNTHETIC); MENTHOL, UNSPECIFIED FORM
Active strength: 110 mg/g; mg/g
NDC exclude flag: No
Listing certified through: 2023-12-31
Current FDA listing: Historical FDA.report record

NDC auxiliary status#

These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.

Current NDC status page 1 of 1 · 1 matching rows.

Dataset, Scope, Product NDC table
Dataset	Scope	Product NDC	Package NDC	Code	Status	Reporting period	Source date
excluded package	package	76168-331	76168-331-18	I	Inactivated by FDA		2026-10-15

Observed NDC auxiliary status history#

This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.

Historic NDC status page 1 of 1 · 18 matching rows.

View current auxiliary records. · View the auxiliary file history.

Captured / source date, Snapshot, Source SHA-256 table
Captured / source date	Snapshot	Source SHA-256
2025-12-14 17:58 UTC · source 2025-12-05	`d630ba8d3edf…`	`732f749b63fb…`
2025-08-27 00:01 UTC · source 2025-08-26	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-04-01 02:39 UTC · source 2025-03-31	`2ef7874e63bc…`	`57b86245f4fa…`
2025-03-28 20:22 UTC · source 2025-03-28	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-22 03:12 UTC · source 2025-03-21	`cfe11265f3b6…`	`090c488252e2…`
2025-03-10 12:48 UTC · source 2025-03-10	`cdf11ea48f46…`	`ba0047e9e063…`
2025-02-02 03:52 UTC · source 2025-01-31	`302b2466d912…`	`e7b80fea0513…`
2025-01-20 13:05 UTC · source 2025-01-20	`ed331223b511…`	`672a5bd82f5f…`
2025-01-11 03:41 UTC · source 2025-01-10	`0efc9e666f02…`	`f202fb6c5f17…`
2024-11-09 02:27 UTC · source 2024-11-08	`ad56d346431e…`	`cc804d4bbf1e…`
2024-10-04 04:10 UTC · source 2024-10-03	`367a005e9d99…`	`383a685ebd0f…`
2024-07-10 04:00 UTC · source 2024-07-09	`557ba5c1ecfa…`	`9c80585c8c6e…`
2024-05-28 21:12 UTC · source 2024-05-28	`8af77b9d5b6f…`	`d9bbb34c5368…`
2024-05-15 03:39 UTC · source 2024-05-14	`834df4deac94…`	`adcc014656a3…`
2024-03-11 06:39 UTC · source 2024-03-08	`1332a3947898…`	`d4bfe170f9cd…`
2022-08-30 03:57 UTC · source 2022-08-29	`fb8cb913e6d1…`	`eb8c232b6be0…`
2022-04-09 23:13 UTC · source 2022-04-08	`86f5da6cb304…`	`a595104c45d7…`
2022-04-04 05:40 UTC · source 2022-04-01	`bd6a592717d7…`	`303034d00443…`

Reported adverse events (FAERS/openFDA)#

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

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
76168-331-18	2024-01-30	C162847	48780-1	d6a99b39-fb52-a426-e053-dadaa90af4c2	Ultra strength pain relief balm
76168-331-18	2022-11-21	C162847	48780-1	d6a99b39-fb52-a426-e053-dadaa90af4c2	Ultra strength pain relief balm
76168-331-18	2022-01-28	C162847	48780-1	d6a99b39-fb52-a426-e053-dadaa90af4c2	Ultra strength pain relief balm

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
76168-331-18	Ultra strength pain relief balmUltra Strength	18 g in 1 JAR	OINTMENT	18		3
76168-331-18	Ultra strength pain relief balmUltra Strength	1 in 1 PACKAGE	OINTMENT	1		3

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
76168-331	ULTRA STRENGTH PAIN RELIEF BALM ULTRA STRENGTH (CAMPHOR (SYNTHETIC) AND MENTHOL) OINTMENT [VELOCITY PHARMA LLC]	3	Legacy NDC, 2 package rows	20221122_5f791159-c388-4c77-8aca-35e4c3f7cacd.zip

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
5TJD82A1ET	CAMPHOR (SYNTHETIC)	76-22-2	CAMPHOR (SYNTHETIC)
L7T10EIP3A	MENTHOL, UNSPECIFIED FORM	1490-04-6	MENTHOL, UNSPECIFIED FORM

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
1089847	camphor 11 % / menthol 11 % Topical Ointment	PSN	5f791159-c388-4c77-8aca-35e4c3f7cacd	3
1089847	camphor 0.11 MG/MG / menthol 0.11 MG/MG Topical Ointment	SCD	5f791159-c388-4c77-8aca-35e4c3f7cacd	3
1089847	camphor 11 % / menthol 11 % Topical Ointment	SY	5f791159-c388-4c77-8aca-35e4c3f7cacd	3

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
76168-331-18	76168033118	1 JAR in 1 PACKAGE (76168-331-18) > 18 g in 1 JAR	1 jar	2020-09-10	0000-00-00	No	No	Current