Food Additives
NDC 43857-0168, Berberis Vulgaris, Chelidonium Majus, Trifolium Pratense, Glycyrrhiza Glabra, Lappa Major, Phytolacca Decandra, Rhamnus Frangula, Rhamnus Purshiana, Stillingia Sylvatica, Xanthoxylum Fraxineum, Arsenicum Album, Belladonna, Lycopodium Clavatum, Natrum Sulphuricum, Phosphoricum Acidum, liquid, from BioActive Nutritional, Inc..
- Product NDC
- 43857-0168
- Status
- Listed
- Labeler
- BioActive Nutritional, Inc.
- Dosage form
- LIQUID
- Route
- ORAL
- Product type
- HUMAN OTC DRUG
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Application
- —
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/43857-0168 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- BERBERIS VULGARIS ROOT BARK3 [hp_X]/mL
- CHELIDONIUM MAJUS3 [hp_X]/mL
- TRIFOLIUM PRATENSE FLOWER3 [hp_X]/mL
- GLYCYRRHIZA GLABRA4 [hp_X]/mL
- ARCTIUM LAPPA ROOT4 [hp_X]/mL
- PHYTOLACCA AMERICANA ROOT4 [hp_X]/mL
- FRANGULA ALNUS BARK4 [hp_X]/mL
- FRANGULA PURSHIANA BARK4 [hp_X]/mL
- STILLINGIA SYLVATICA ROOT4 [hp_X]/mL
- ZANTHOXYLUM AMERICANUM BARK4 [hp_X]/mL
- ARSENIC TRIOXIDE12 [hp_X]/mL
- ATROPA BELLADONNA WHOLE12 [hp_X]/mL
- LYCOPODIUM CLAVATUM SPORE12 [hp_X]/mL
- SODIUM SULFATE12 [hp_X]/mL
- PHOSPHORIC ACID12 [hp_X]/mL
Pharmacologic classes
Allergens [CS]; Cell-mediated Immunity [PE]; Dietary Proteins [CS]; Increased Histamine Release [PE]; Non-Standardized Food Allergenic Extract [EPC]; Non-Standardized Plant Allergenic Extract [EPC]; Plant Proteins [CS]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 43857-0168-1 | 43857016801 | 30 mL in 1 BOTTLE, DROPPER (43857-0168-1) |
Linked data
RxNorm, label and prices
RxNorm concepts
RxNorm links no concept to this product's packages.
Related lookups
No FDA label, Medicare Part B payment limit or NADAC price is linked to this product.
Use it
Look up 43857-0168 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/43857-0168 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 43857-0168. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.