Renes Betula

Product NDC

48951-8446

11-digit product format

489518446

Labeler code

48951

Product ID

48951-8446_5e4c9171-cfc0-e822-e063-6294a90a707f

Type

HUMAN OTC DRUG

Nonproprietary name

Renes Betula

Dosage form

PELLET

Route

ORAL

Labeler

Uriel Pharmacy Inc.

Marketing category

UNAPPROVED HOMEOPATHIC

Marketing start

2009-09-01

Substance

ONONIS REPENS ROOT; PARSLEY; CAPSELLA BURSA-PASTORIS; ARCTOSTAPHYLOS UVA-URSI LEAF; SOLIDAGO VIRGAUREA FLOWERING TOP; BETULA PUBESCENS LEAF; EQUISETUM ARVENSE TOP; CYTISUS SCOPARIUS FLOWERING TOP; PORK KIDNEY; COPPER; ELYMUS REPENS ROOT

Active strength

3; 3; 3; 3; 3; 5; 4; 4; 5; 9; 5 [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1

Pharmacologic classes

Allergens [CS], Allergens [CS], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Copper [CS], Copper-containing Intrauterine Device [EPC], Decreased Embryonic Implantation [PE], Decreased Sperm Motility [PE], Dietary Proteins [CS], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Inhibit Ovum Fertilization [PE], Non-Standardized Food Allergenic Extract [EPC], Non-Standardized Plant Allergenic Extract [EPC], Plant Proteins [CS], Vegetable Proteins [CS]

NDC exclude flag

No

Listing certified through

2027-12-31

Current FDA listing

Yes