Chronagesic
NDC 43742-2207, Alpha-Lipoicum Acidum, Apiolum, Arnica Montana, Cartilago Suis, Cinnamomum, Dulcamara, Funiculus Umbilicalis Suis, Nadidum, Natrum Oxalaceticum, Pantothenic Acid, Placenta Totalis Suis, Piper Nigrum, Rhus Tox, Sanguinaria Canadensis, Sulphur, Silicea, Symphytum Officinale, Thuja Occidentalis, liquid, from Deseret Biologicals, Inc..
- Product NDC
- 43742-2207
- Status
- Listed
- Labeler
- Deseret Biologicals, 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/43742-2207 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- ALPHA LIPOIC ACID8 [hp_X]/mL
- APIOLE (PARSLEY)16 [hp_C]/mL
- ARNICA MONTANA WHOLE3 [hp_X]/mL
- SUS SCROFA CARTILAGE8 [hp_X]/mL
- CINNAMON6 [hp_X]/mL
- SOLANUM DULCAMARA TOP6 [hp_X]/mL
- SUS SCROFA UMBILICAL CORD6 [hp_X]/mL
- NADIDE6 [hp_X]/mL
- SODIUM DIETHYL OXALACETATE6 [hp_X]/mL
- PANTOTHENIC ACID6 [hp_X]/mL
- SUS SCROFA PLACENTA6 [hp_X]/mL
- GREEN PEPPERCORN6 [hp_X]/mL
- TOXICODENDRON PUBESCENS LEAF8 [hp_X]/mL
- SANGUINARIA CANADENSIS ROOT6 [hp_X]/mL
- SULFUR6 [hp_X]/mL
- SILICON DIOXIDE8 [hp_X]/mL
- COMFREY ROOT8 [hp_X]/mL
- THUJA OCCIDENTALIS LEAFY TWIG12 [hp_X]/mL
Pharmacologic classes
Allergens [CS]; Cell-mediated Immunity [PE]; Dietary Proteins [CS]; Food Additives [CS]; Increased Histamine Release [PE]; Non-Standardized Food Allergenic Extract [EPC]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 43742-2207-1 | 43742220701 | 30 mL in 1 BOTTLE, DROPPER (43742-2207-1) |
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 43742-2207 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/43742-2207 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 43742-2207. 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.