Reynoutria Lyme

Product NDC: 48951-8396
Requested package NDC: 48951-8396-3
11-digit product format: 489518396
Labeler code: 48951
Product ID: 48951-8396_eac885e5-e8fe-a7c9-e053-2995a90a566a
Type: HUMAN OTC DRUG
Nonproprietary name: Reynoutria Lyme
Dosage form: LIQUID
Route: ORAL
Labeler: Uriel Pharmacy, Inc.
Marketing category: UNAPPROVED HOMEOPATHIC
Marketing start: 2009-09-01
Marketing end: 0000-00-00
Substance: APIS MELLIFERA; ASTRAGALUS CHINENSIS SEED; ASTRAGALUS PROPINQUUS ROOT; COPPER; DIPSACUS FULLONUM WHOLE; GOLD; HELLEBORUS NIGER ROOT; REYNOUTRIA JAPONICA LEAF; SILICON DIOXIDE; SILVER
Active strength: 21 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
Pharmacologic classes: Allergens [CS], Allergens [CS], Bee Venoms [CS], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Copper [CS], Copper-containing Intrauterine Device [EPC], Decreased Embryonic Implantation [PE], Decreased Sperm Motility [PE], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Inhibit Ovum Fertilization [PE], Standardized Chemical Allergen [EPC], Standardized Insect Venom Allergenic Extract [EPC]
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	48951-8396	48951-8396-3	I	Inactivated by FDA		2026-10-05

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

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
c599c4a0-705d-4ebb-ab1f-977af038f96a	Product name	1	20251124

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
48951-8396-3	Reynoutria Lyme	60 mL in 1 BOTTLE, GLASS	LIQUID	60		1

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
48951-8396	REYNOUTRIA LYME LIQUID [URIEL PHARMACY, INC.]	1	Legacy NDC, 1 package rows	20221012_eac885e5-e8fd-a7c9-e053-2995a90a566a.zip

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
7S82P3R43Z	APIS MELLIFERA		APIS MELLIFERA
U046B39ADE	ASTRAGALUS CHINENSIS SEED		ASTRAGALUS CHINENSIS SEED
922OP8YUPF	ASTRAGALUS PROPINQUUS ROOT		ASTRAGALUS PROPINQUUS ROOT
789U1901C5	COPPER	7440-50-8	COPPER
1FT87R544S	DIPSACUS FULLONUM WHOLE		DIPSACUS FULLONUM WHOLE
79Y1949PYO	GOLD	7440-57-5	GOLD
608DGJ6815	HELLEBORUS NIGER ROOT		HELLEBORUS NIGER ROOT
2540B7G25G	REYNOUTRIA JAPONICA LEAF		REYNOUTRIA JAPONICA LEAF
ETJ7Z6XBU4	SILICON DIOXIDE	7631-86-9	SILICON DIOXIDE
3M4G523W1G	SILVER	7440-22-4	SILVER

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
48951-8396-3	48951839603	60 mL in 1 BOTTLE, GLASS (48951-8396-3)	60 ml	2009-09-01	0000-00-00	No	No	Current