Novarnica Foot Pain Reliever

Product NDC: 61871-005
11-digit product format: 618710005
Labeler code: 61871
Product ID: 61871-005_84dddf7a-5cd1-449a-954e-aae4907b1376
Type: HUMAN OTC DRUG
Nonproprietary name: camphor and menthol
Dosage form: SPRAY
Route: TOPICAL
Labeler: Xcentrik Inc.
Application: part348
Marketing category: OTC MONOGRAPH NOT FINAL
Marketing start: 2015-04-01
Marketing end: 0000-00-00
Substance: CAMPHOR (NATURAL); MENTHOL
Active strength: 4 g/100mL; g/100mL
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 · 2 matching rows.

Dataset, Scope, Product NDC table
Dataset	Scope	Product NDC	Package NDC	Code	Status	Reporting period	Source date
excluded product	product	61871-005		I	Inactivated by FDA		2026-10-16
excluded package	package	61871-005	61871-005-01	I	Inactivated by FDA		2026-10-16

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 · 30 matching rows.

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

Captured / source date, Dataset, Scope table
Captured / source date	Dataset	Scope	Package NDC	Snapshot	Source SHA-256
2025-12-14 17:58 UTC · source 2025-12-05	excluded product	product		`d630ba8d3edf…`	`732f749b63fb…`
2025-12-14 17:58 UTC · source 2025-12-05	excluded package	package	61871-005-01	`d630ba8d3edf…`	`732f749b63fb…`
2025-08-27 00:01 UTC · source 2025-08-26	excluded product	product		`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-08-27 00:01 UTC · source 2025-08-26	excluded package	package	61871-005-01	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-04-01 02:39 UTC · source 2025-03-31	excluded product	product		`2ef7874e63bc…`	`57b86245f4fa…`
2025-04-01 02:39 UTC · source 2025-03-31	excluded package	package	61871-005-01	`2ef7874e63bc…`	`57b86245f4fa…`
2025-03-28 20:22 UTC · source 2025-03-28	excluded product	product		`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-28 20:22 UTC · source 2025-03-28	excluded package	package	61871-005-01	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-22 03:12 UTC · source 2025-03-21	excluded product	product		`cfe11265f3b6…`	`090c488252e2…`
2025-03-22 03:12 UTC · source 2025-03-21	excluded package	package	61871-005-01	`cfe11265f3b6…`	`090c488252e2…`
2025-03-10 12:48 UTC · source 2025-03-10	excluded product	product		`cdf11ea48f46…`	`ba0047e9e063…`
2025-03-10 12:48 UTC · source 2025-03-10	excluded package	package	61871-005-01	`cdf11ea48f46…`	`ba0047e9e063…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded product	product		`302b2466d912…`	`e7b80fea0513…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded package	package	61871-005-01	`302b2466d912…`	`e7b80fea0513…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded product	product		`ed331223b511…`	`672a5bd82f5f…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded package	package	61871-005-01	`ed331223b511…`	`672a5bd82f5f…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded product	product		`0efc9e666f02…`	`f202fb6c5f17…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded package	package	61871-005-01	`0efc9e666f02…`	`f202fb6c5f17…`
2024-11-09 02:27 UTC · source 2024-11-08	excluded product	product		`ad56d346431e…`	`cc804d4bbf1e…`
2024-11-09 02:27 UTC · source 2024-11-08	excluded package	package	61871-005-01	`ad56d346431e…`	`cc804d4bbf1e…`
2024-10-04 04:10 UTC · source 2024-10-03	excluded product	product		`367a005e9d99…`	`383a685ebd0f…`
2024-10-04 04:10 UTC · source 2024-10-03	excluded package	package	61871-005-01	`367a005e9d99…`	`383a685ebd0f…`
2024-07-10 04:00 UTC · source 2024-07-09	excluded product	product		`557ba5c1ecfa…`	`9c80585c8c6e…`
2024-07-10 04:00 UTC · source 2024-07-09	excluded package	package	61871-005-01	`557ba5c1ecfa…`	`9c80585c8c6e…`
2024-05-28 21:12 UTC · source 2024-05-28	excluded product	product		`8af77b9d5b6f…`	`d9bbb34c5368…`
2024-05-28 21:12 UTC · source 2024-05-28	excluded package	package	61871-005-01	`8af77b9d5b6f…`	`d9bbb34c5368…`
2024-05-15 03:39 UTC · source 2024-05-14	excluded product	product		`834df4deac94…`	`adcc014656a3…`
2024-05-15 03:39 UTC · source 2024-05-14	excluded package	package	61871-005-01	`834df4deac94…`	`adcc014656a3…`
2024-03-11 06:39 UTC · source 2024-03-08	excluded product	product		`1332a3947898…`	`d4bfe170f9cd…`
2024-03-11 06:39 UTC · source 2024-03-08	excluded package	package	61871-005-01	`1332a3947898…`	`d4bfe170f9cd…`

Reported adverse events (FAERS/openFDA)#

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

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
6c13b22c-b3ba-4127-b768-0132dd5ab0d1	Product name	1	20230829

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
61871-005-01	2023-07-28	C162847	48780-1	0191ceaa-6fbd-198a-e063-dbdaa90aec3e	33faf91e-0ffe-499f-b190-1b7969f1231a

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
61871-005-01	Novarnica Foot Pain Reliever	65 mL in 1 BOTTLE	SPRAY	65		7
61871-005-01	Novarnica Foot Pain Reliever	1 in 1 CARTON	SPRAY	1		7

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
CAMPHOR (NATURAL)	ACTIVE INGREDIENT	N20HL7Q941	NOVARNICA FOOT PAIN RELIEVER (CAMPHOR AND MENTHOL) SPRAY [XCENTRIK INC.]	1
MENTHOL	ACTIVE INGREDIENT	L7T10EIP3A	NOVARNICA FOOT PAIN RELIEVER (CAMPHOR AND MENTHOL) SPRAY [XCENTRIK INC.]	1
CAMPHOR (NATURAL)	ACTIVE MOIETY	N20HL7Q941	NOVARNICA FOOT PAIN RELIEVER (CAMPHOR AND MENTHOL) SPRAY [XCENTRIK INC.]	1
MENTHOL	ACTIVE MOIETY	L7T10EIP3A	NOVARNICA FOOT PAIN RELIEVER (CAMPHOR AND MENTHOL) SPRAY [XCENTRIK INC.]	1
ARNICA MONTANA FLOWER	INACTIVE INGREDIENT	OZ0E5Y15PZ	NOVARNICA FOOT PAIN RELIEVER (CAMPHOR AND MENTHOL) SPRAY [XCENTRIK INC.]	1
CLOVE OIL	INACTIVE INGREDIENT	578389D6D0	NOVARNICA FOOT PAIN RELIEVER (CAMPHOR AND MENTHOL) SPRAY [XCENTRIK INC.]	1
EUCALYPTUS OIL	INACTIVE INGREDIENT	2R04ONI662	NOVARNICA FOOT PAIN RELIEVER (CAMPHOR AND MENTHOL) SPRAY [XCENTRIK INC.]	1
ISOPROPYL ALCOHOL	INACTIVE INGREDIENT	ND2M416302	NOVARNICA FOOT PAIN RELIEVER (CAMPHOR AND MENTHOL) SPRAY [XCENTRIK INC.]	1
PEPPERMINT OIL	INACTIVE INGREDIENT	AV092KU4JH	NOVARNICA FOOT PAIN RELIEVER (CAMPHOR AND MENTHOL) SPRAY [XCENTRIK INC.]	1
POLYSORBATE 20	INACTIVE INGREDIENT	7T1F30V5YH	NOVARNICA FOOT PAIN RELIEVER (CAMPHOR AND MENTHOL) SPRAY [XCENTRIK INC.]	1
WATER	INACTIVE INGREDIENT	059QF0KO0R	NOVARNICA FOOT PAIN RELIEVER (CAMPHOR AND MENTHOL) SPRAY [XCENTRIK INC.]	1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
61871-005	NOVARNICA FOOT PAIN RELIEVER (CAMPHOR AND MENTHOL) SPRAY [XCENTRIK INC.]	7	Legacy NDC, 2 package rows	20221221_33faf91e-0ffe-499f-b190-1b7969f1231a.zip

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
N20HL7Q941	CAMPHOR (NATURAL)	464-49-3	CAMPHOR (NATURAL)

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
1043494	camphor 4 % / menthol 8 % Topical Spray	PSN	33faf91e-0ffe-499f-b190-1b7969f1231a	7
1043494	camphor 40 MG/ML / menthol 80 MG/ML Topical Spray	SCD	33faf91e-0ffe-499f-b190-1b7969f1231a	7
1043494	camphor 4 % / menthol 8 % Topical Spray	SY	33faf91e-0ffe-499f-b190-1b7969f1231a	7

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
61871-005-01	61871000501	1 BOTTLE in 1 CARTON (61871-005-01) > 65 mL in 1 BOTTLE	1 bottle	2015-04-01	0000-00-00	No	No	Current