Eupatorium comp.

Product NDC: 48951-4049
11-digit product format: 489514049
Labeler code: 48951
Product ID: 48951-4049_6c6cf5c9-fd8c-c0ca-e053-2a91aa0a1044
Type: HUMAN OTC DRUG
Nonproprietary name: Eupatorium comp.
Dosage form: LIQUID
Route: ORAL
Labeler: Uriel Pharmacy Inc.
Marketing category: UNAPPROVED HOMEOPATHIC
Marketing start: 2009-09-01
Marketing end: 0000-00-00
Substance: EUPATORIUM PERFOLIATUM FLOWERING TOP; ACONITUM NAPELLUS; BRYONIA ALBA ROOT; PHOSPHORUS; LACHESIS MUTA VENOM
Active strength: 5 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [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	48951-4049		I	Inactivated by FDA		2026-10-05
excluded package	package	48951-4049	48951-4049-1	I	Inactivated by FDA		2026-10-05

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

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
48951-4049-1	Eupatorium comp.	1 mL in 1 AMPULE	LIQUID	1		3
48951-4049-1	Eupatorium comp.	10 in 1 BOX	LIQUID	10		3

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
ACONITUM NAPELLUS	ACTIVE INGREDIENT	U0NQ8555JD	EUPATORIUM COMP. LIQUID [URIEL PHARMACY INC.]	1
BRYONIA ALBA ROOT	ACTIVE INGREDIENT	T7J046YI2B	EUPATORIUM COMP. LIQUID [URIEL PHARMACY INC.]	1
EUPATORIUM PERFOLIATUM FLOWERING TOP	ACTIVE INGREDIENT	1W0775VX6E	EUPATORIUM COMP. LIQUID [URIEL PHARMACY INC.]	1
LACHESIS MUTA VENOM	ACTIVE INGREDIENT	VSW71SS07I	EUPATORIUM COMP. LIQUID [URIEL PHARMACY INC.]	1
PHOSPHORUS	ACTIVE INGREDIENT	27YLU75U4W	EUPATORIUM COMP. LIQUID [URIEL PHARMACY INC.]	1
ACONITUM NAPELLUS	ACTIVE MOIETY	U0NQ8555JD	EUPATORIUM COMP. LIQUID [URIEL PHARMACY INC.]	1
BRYONIA ALBA ROOT	ACTIVE MOIETY	T7J046YI2B	EUPATORIUM COMP. LIQUID [URIEL PHARMACY INC.]	1
EUPATORIUM PERFOLIATUM FLOWERING TOP	ACTIVE MOIETY	1W0775VX6E	EUPATORIUM COMP. LIQUID [URIEL PHARMACY INC.]	1
LACHESIS MUTA VENOM	ACTIVE MOIETY	VSW71SS07I	EUPATORIUM COMP. LIQUID [URIEL PHARMACY INC.]	1
PHOSPHORUS	ACTIVE MOIETY	27YLU75U4W	EUPATORIUM COMP. LIQUID [URIEL PHARMACY INC.]	1
SODIUM CHLORIDE	INACTIVE INGREDIENT	451W47IQ8X	EUPATORIUM COMP. LIQUID [URIEL PHARMACY INC.]	1
WATER	INACTIVE INGREDIENT	059QF0KO0R	EUPATORIUM COMP. LIQUID [URIEL PHARMACY INC.]	1

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
48951-4049	EUPATORIUM COMP. LIQUID [URIEL PHARMACY INC.]	3	Legacy NDC, 2 package rows	20180518_2ff553f5-0b10-4233-8acf-cf2d621353d1.zip

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
1W0775VX6E	EUPATORIUM PERFOLIATUM FLOWERING TOP		EUPATORIUM PERFOLIATUM FLOWERING TOP
U0NQ8555JD	ACONITUM NAPELLUS		ACONITUM NAPELLUS
T7J046YI2B	BRYONIA ALBA ROOT		BRYONIA ALBA ROOT
27YLU75U4W	PHOSPHORUS	7723-14-0	PHOSPHORUS
VSW71SS07I	LACHESIS MUTA VENOM		LACHESIS MUTA VENOM

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
48951-4049-1	48951404901	10 AMPULE in 1 BOX (48951-4049-1) > 1 mL in 1 AMPULE	10 ampule	2009-09-01	0000-00-00	No	No	Current