NDC 48951-3039 – Cartilago Betula

Betula Pubescens Leaf 5 [hp_X]/mL; Aconitum Napellus 6 [hp_X]/mL; Arnica Montana 6 [hp_X]/mL; Bos Taurus Cartilage 8 [hp_X]/mL; Tin 8 [hp_X]/mL; Gold 10… · Liquid · Oral

Human Otc Drug

Product NDC48951-3039

Product details

Brand name
Cartilago Betula
Generic name
Cartilago Betula
Labeler
Uriel Pharmacy Inc.
Dosage form
Liquid
Route
Oral
Marketing category
UNAPPROVED HOMEOPATHIC
Marketed since
September 1, 2009
Listing expires
December 31, 2026
Pharmacologic class
Non-Standardized Food Allergenic Extract; Standardized Chemical Allergen

Active ingredients

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

Package NDC codes (1)

Package NDCDescriptionSince
48951-3039-110 AMPULE in 1 BOX (48951-3039-1) / 1 mL in 1 AMPULESep 1, 2009

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