48951-8379 : Secale Betula Oral Liquid
| NDC: | 48951-8379 |
| Labeler: | Uriel Pharmacy Inc. |
| Product Type: | Human OTC Drug |
| Drug Name: | Secale Betula |
| Dosage Form: | Oral Liquid |
| Rev. Date: |
NDC Package Codes:
- 48951-8379-1: 10 AMPULE IN 1 BOX (48951‑8379‑1) > 1 ML IN 1 AMPULE
Active Ingredients:
- Arnica Montana
- Betula Pendula Leaf
- Claviceps Purpurea Sclerotium
- Lead Sulfide
- Bos Taurus Eye
- Betula Pendula Bark
- Levisticum Officinale Root
- Tobacco Leaf
Dosage Strength:
- 12 [hp_X]/mL
- 3 [hp_X]/mL
- 6 [hp_X]/mL
- 8 [hp_X]/mL
- 8 [hp_X]/mL
- 4 [hp_X]/mL
- 6 [hp_X]/mL
- 6 [hp_X]/mL
Pharmaceutical Classes:
- Allergens [CS]
- Cell-mediated Immunity [PE]
- Increased Histamine Release [PE]
- Increased IgG Production [PE]
- Non-Standardized Plant Allergenic Extract [EPC]
- Plant Proteins [CS]
Related Products:
Based on records with the same trade name.- 48951-8175 Secale Betula Oral Pellet by Uriel Pharmacy Inc.
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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.
