Arnica e rad. 20X

Product NDC: 48951-1336
11-digit product format: 489511336
Labeler code: 48951
Product ID: 48951-1336_983203fc-5c51-2888-e053-2995a90a6d67
Type: HUMAN OTC DRUG
Nonproprietary name: Arnica e rad. 20X
Dosage form: LIQUID
Route: ORAL
Labeler: Uriel Pharmacy Inc.
Marketing category: UNAPPROVED HOMEOPATHIC
Marketing start: 2009-09-01
Marketing end: 0000-00-00
Substance: ARNICA MONTANA ROOT
Active strength: 20 [hp_X]/mL
NDC exclude flag: No
Listing certified through: 2020-12-31
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	48951-1336		I	Inactivated by FDA		2026-08-10
excluded package	package	48951-1336	48951-1336-1	I	Inactivated by FDA		2026-08-10

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, Dataset, Scope table
Captured / source date	Dataset	Scope	Package NDC	Code	Status	Snapshot	Source SHA-256
2025-12-14 17:58 UTC · source 2025-12-05	excluded product	product		I	Inactivated by FDA	`d630ba8d3edf…`	`732f749b63fb…`
2025-12-14 17:58 UTC · source 2025-12-05	excluded package	package	48951-1336-1	I	Inactivated by FDA	`d630ba8d3edf…`	`732f749b63fb…`
2025-08-27 00:01 UTC · source 2025-08-26	excluded product	product		I	Inactivated by FDA	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-08-27 00:01 UTC · source 2025-08-26	excluded package	package	48951-1336-1	I	Inactivated by FDA	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-04-01 02:39 UTC · source 2025-03-31	excluded product	product		I	Inactivated by FDA	`2ef7874e63bc…`	`57b86245f4fa…`
2025-04-01 02:39 UTC · source 2025-03-31	excluded package	package	48951-1336-1	I	Inactivated by FDA	`2ef7874e63bc…`	`57b86245f4fa…`
2025-03-28 20:22 UTC · source 2025-03-28	excluded product	product		I	Inactivated by FDA	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-28 20:22 UTC · source 2025-03-28	excluded package	package	48951-1336-1	I	Inactivated by FDA	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-22 03:12 UTC · source 2025-03-21	excluded product	product		I	Inactivated by FDA	`cfe11265f3b6…`	`090c488252e2…`
2025-03-22 03:12 UTC · source 2025-03-21	excluded package	package	48951-1336-1	I	Inactivated by FDA	`cfe11265f3b6…`	`090c488252e2…`
2025-03-10 12:48 UTC · source 2025-03-10	excluded product	product		I	Inactivated by FDA	`cdf11ea48f46…`	`ba0047e9e063…`
2025-03-10 12:48 UTC · source 2025-03-10	excluded package	package	48951-1336-1	I	Inactivated by FDA	`cdf11ea48f46…`	`ba0047e9e063…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded product	product		U	Excluded because listing certification expired	`302b2466d912…`	`e7b80fea0513…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded package	package	48951-1336-1	U	Excluded because listing certification expired	`302b2466d912…`	`e7b80fea0513…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded product	product		U	Excluded because listing certification expired	`ed331223b511…`	`672a5bd82f5f…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded package	package	48951-1336-1	U	Excluded because listing certification expired	`ed331223b511…`	`672a5bd82f5f…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded product	product		U	Excluded because listing certification expired	`0efc9e666f02…`	`f202fb6c5f17…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded package	package	48951-1336-1	U	Excluded because listing certification expired	`0efc9e666f02…`	`f202fb6c5f17…`

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
48951-1336-1	2025-01-30	C162847	48780-1	2cef2736-597a-d83d-e063-dadaa90ab31f	Arnica e rad. 20X

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
48951-1336-1	Arnica e rad. 20X	1 mL in 1 AMPULE	LIQUID	1		3
48951-1336-1	Arnica e rad. 20X	10 in 1 BOX	LIQUID	10		3

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
ARNICA MONTANA ROOT	ACTIVE INGREDIENT	MUE8Y11327	ARNICA E RAD. 20 LIQUID [URIEL PHARMACY INC.]	1
ARNICA MONTANA ROOT	ACTIVE MOIETY	MUE8Y11327	ARNICA E RAD. 20 LIQUID [URIEL PHARMACY INC.]	1
SODIUM CHLORIDE	INACTIVE INGREDIENT	451W47IQ8X	ARNICA E RAD. 20 LIQUID [URIEL PHARMACY INC.]	1
WATER	INACTIVE INGREDIENT	059QF0KO0R	ARNICA E RAD. 20 LIQUID [URIEL PHARMACY INC.]	1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
48951-1336	ARNICA E RAD. 20X LIQUID [URIEL PHARMACY INC.]	3	Legacy NDC, 2 package rows	20191126_8b06f2e3-595d-4d22-9323-900ab6dabf6b.zip

UNII, Preferred term, Matched term table
UNII	Preferred term	Matched term
MUE8Y11327	ARNICA MONTANA ROOT	ARNICA MONTANA ROOT

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
48951-1336-1	48951133601	10 AMPULE in 1 BOX (48951-1336-1) > 1 mL in 1 AMPULE	10 ampule	2009-09-01	0000-00-00	No	No	Current