NDC product
GUNA-SPASM
NDC 17089-348 · Guna spa
Key facts
| Product NDC | 17089-348 |
|---|---|
| Proprietary name | GUNA-SPASM |
| Nonproprietary name | atropine sulfate - berberis vulgaris root bark - chelidonium majus - cobalt - cultivated mushroom - gelsemium sempervirens root - interleukin-10 - magnesium - melatonin - metenkefalin - sus scrofa… |
| Substances | CULTIVATED MUSHROOM, ANTI-INTERLEUKIN-1.ALPHA. IMMUNOGLOBULIN G RABBIT, ATROPINE SULFATE, BERBERIS VULGARIS ROOT BARK, METENKEFALIN, CHELIDONIUM MAJUS, COBALT, WATERMELON, GELSEMIUM SEMPERVIRENS ROOT, INTERLEUKIN-10, MAGNESIUM, MELATONIN and 2 more |
| Dosage form | SOLUTION/ DROPS |
| Route | ORAL |
| Labeler | Guna spa |
| Product type | HUMAN OTC DRUG |
| Marketing category | UNAPPROVED HOMEOPATHIC |
| Pharmacologic classes | Allergens [CS], Anticholinergic [EPC], Cell-mediated Immunity [PE], Cholinergic Antagonists [MoA], Cholinergic Muscarinic Antagonist [EPC], Cholinergic Muscarinic Antagonists [MoA] and 6 more |
| Marketing start | Apr 16, 2008 |
| 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: