50181-0014 : Biotox Para Oral Liquid
| NDC: | 50181-0014 |
| Labeler: | The Wellness Center |
| Product Type: | Human OTC Drug |
| Drug Name: | Biotox Para |
| Dosage Form: | Oral Liquid |
| Rev. Date: |
NDC Package Codes:
- 50181-0014-1: 30 ML IN 1 BOTTLE, DROPPER (50181‑0014‑1)
Active Ingredients:
- Candida Albicans
- Horseradish
- Plasmodium Malariae
- Taraxacum Officinale
- Toxoplasma Gondii
- Trichinella Spiralis
- Trichophyton Rubrum
- Vibrio Cholerae
Dosage Strength:
- 30 [hp_X]/mL
- 3 [hp_X]/mL
- 12 [hp_C]/mL
- 8 [hp_C]/mL
- 12 [hp_X]/mL
- 30 [hp_X]/mL
- 200 [hp_C]/mL
- 30 [hp_X]/mL
Pharmaceutical Classes:
- Allergens [CS]
- Allergens [CS]
- Cell-mediated Immunity [PE]
- Dietary Proteins [CS]
- Food Additives [CS]
- Fungal Proteins [CS]
- Increased Histamine Release [PE]
- Increased IgG Production [PE]
- Non-Standardized Food Allergenic Extract [EPC]
- Non-Standardized Fungal Allergenic Extract [EPC]
- Non-Standardized Plant Allergenic Extract [EPC]
- Plant Proteins [CS]
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.
