NDC product
GUNA PAIN MANAGEMENT
NDC 17089-465 · Guna spa
Key facts
| Product NDC | 17089-465 |
|---|---|
| Proprietary name | GUNA PAIN MANAGEMENT |
| Nonproprietary name | achillea millefolium whole - bellis perennis whole - matricaria chamomilla whole - toxicodendron pubescens whole - ruta graveolens flowering top - comfrey root - apis mellifera - bryonia alba root… |
| Substances | BRYONIA ALBA ROOT, HISTAMINE DIHYDROCHLORIDE, HYPERICUM PERFORATUM, ARNICA MONTANA WHOLE, PORK LIVER, BELLIS PERENNIS WHOLE, MATRICARIA CHAMOMILLA WHOLE, TOXICODENDRON PUBESCENS LEAF, RUTA GRAVEOLENS FLOWERING TOP, KALMIA LATIFOLIA LEAF, ACHILLEA MILLEFOLIUM WHOLE, COMFREY ROOT and 1 more |
| Dosage form | SOLUTION/ DROPS |
| Route | ORAL |
| Labeler | Guna spa |
| Product type | HUMAN OTC DRUG |
| Marketing category | UNAPPROVED HOMEOPATHIC |
| Pharmacologic classes | Allergens [CS], Bee Venoms [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Standardized Insect Venom Allergenic Extract [EPC] |
| Marketing start | Sep 24, 2020 |
| Listing certified through | Dec 31, 2027 |
At a glance
- 1–9 Package NDCs
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About National Drug Codes (NDC)
The National Drug Code (NDC) is the FDA's product identifier for drugs; the product NDC identifies the labeler and product, and each package adds a package code.
Source: U.S. Food and Drug Administration (FDA), National Drug Code Directory · Source date: