NDC 48951-8125 – Renes Betula

Elymus Repens Root 4 [hp_X]/mL; Ononis Repens Root 2 [hp_X]/mL; Parsley 2 [hp_X]/mL; Capsella Bursa-pastoris 2 [hp_X]/mL; Arctostaphylos Uva-ursi Leaf 2… · Liquid · Oral

Human Otc Drug

Product NDC48951-8125

Product details

Brand name
Renes Betula
Generic name
Renes Betula
Labeler
Uriel Pharmacy Inc.
Dosage form
Liquid
Route
Oral
Marketing category
UNAPPROVED HOMEOPATHIC
Marketed since
September 1, 2009
Listing expires
December 31, 2027
Pharmacologic class
Copper-containing Intrauterine Device; Non-Standardized Food Allergenic Extract; Non-Standardized Plant Allergenic Extract

Active ingredients

Uses, dosage, side effects and warnings for Renes Betula →

Package NDC codes (1)

Package NDCDescriptionSince
48951-8125-360 mL in 1 BOTTLE, DROPPER (48951-8125-3)Sep 1, 2009