Cartilago Betula
Cartilago Betula is listed in the FDA National Drug Code directory with 3 NDC codes, marketed under brand name including Cartilago Betula. Available dosage forms: cream, liquid, pellet.
Drug Details
- Generic Name
- Cartilago Betula
- Brand Names
- Cartilago Betula
- Application Number
- Sponsor
- Uriel Pharmacy Inc.
- NDC Codes
- 3
- Dosage Forms
- CREAM, LIQUID, PELLET
- Routes
- TOPICAL, ORAL
- Active Ingredients
- ONION, BETULA PUBESCENS LEAF, ACONITUM NAPELLUS, ARNICA MONTANA, BOS TAURUS CARTILAGE, FORMICA RUFA, TIN, GOLD
Indications and Usage
Directions: FOR TOPICAL USE ONLY.
Warnings
Warnings: Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated. Do not use if allergic to any ingredient. Consult a doctor before use for serious conditions, if conditions worsen or persist, or accidental ingestion occurs. If pregnant or nursing, consult a doctor before use. Avoid contact with eyes. Do not use if safety seal is broken or missing.