NDC 48951-2149 – Birch Juniper

Juniper Berry 1 [hp_X]/mL; Betula Pendula Bark 1 [hp_X]/mL · Liquid · Oral

Human Otc Drug

Product NDC48951-2149

Product details

Brand name
Birch Juniper
Generic name
Birch Juniper
Labeler
Uriel Pharmacy Inc
Dosage form
Liquid
Route
Oral
Marketing category
UNAPPROVED HOMEOPATHIC
Marketed since
November 3, 2021
Listing expires
December 31, 2026
Pharmacologic class
Non-Standardized Food Allergenic Extract; Non-Standardized Plant Allergenic Extract

Active ingredients

Uses, dosage, side effects and warnings for Birch Juniper →

Package NDC codes (1)

Package NDCDescriptionSince
48951-2149-9240 mL in 1 BOTTLE, GLASS (48951-2149-9)Nov 3, 2021