48951-3039 : Cartilago Betula Oral Liquid
| NDC: | 48951-3039 |
| Labeler: | Uriel Pharmacy Inc. |
| Product Type: | Human OTC Drug |
| Drug Name: | Cartilago Betula |
| Dosage Form: | Oral Liquid |
| Rev. Date: |
NDC Package Codes:
- 48951-3039-1: 10 AMPULE IN 1 BOX (48951‑3039‑1) > 1 ML IN 1 AMPULE
Active Ingredients:
- Aconitum Napellus
- Arnica Montana
- Betula Pubescens Leaf
- Bos Taurus Cartilage
- Formica Rufa
- Gold
- Onion
- Tin
Dosage Strength:
- 6 [hp_X]/mL
- 6 [hp_X]/mL
- 5 [hp_X]/mL
- 8 [hp_X]/mL
- 17 [hp_X]/mL
- 10 [hp_X]/mL
- 17 [hp_X]/mL
- 8 [hp_X]/mL
Pharmaceutical Classes:
- Allergens [CS]
- Allergens [CS]
- Cell-mediated Immunity [PE]
- Dietary Proteins [CS]
- Increased Histamine Release [PE]
- Non-Standardized Food Allergenic Extract [EPC]
- Standardized Chemical Allergen [EPC]
- Vegetable Proteins [CS]
Related Products:
Based on records with the same trade name.- 48951-3040 Cartilago Betula Topical Cream by Uriel Pharmacy Inc.
- 48951-3041 Cartilago Betula Oral Pellet by Uriel Pharmacy Inc.
NDC QR Code
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Note: The RxChat NDC Database uses publicly available data from the FDA and the U.S. National Library of Medicine (NLM); The NLM is not responsible for the data presented and does not endorse or recommend this or any other product. While we make every effort to ensure that the information presented is accurate, you should assume that all results are unvalidated. To report any errors or inconsistencies please contact us.
