NDC product
GUNA-COUGH
NDC 17089-453 · Guna spa
Key facts
| Product NDC | 17089-453 |
|---|---|
| Proprietary name | GUNA-COUGH |
| Nonproprietary name | ALTHAEA OFFICINALIS LEAF - ANTIMONY POTASSIUM TARTRATE - BRYONIA ALBA ROOT - CETRARIA ISLANDICA SUBSP. ISLANDICA - COCHINEAL - COPPER - DROSERA ROTUNDIFOLIA - ECHINACEA ANGUSTIFOLIA - GARDEN THYME… |
| Substances | ALTHAEA OFFICINALIS LEAF, ANTIMONY POTASSIUM TARTRATE, BRYONIA ALBA ROOT, CETRARIA ISLANDICA SUBSP. ISLANDICA, COCHINEAL, COPPER, DROSERA ROTUNDIFOLIA, ECHINACEA ANGUSTIFOLIA, PLANTAGO MAJOR, LOBARIA PULMONARIA, THYME |
| Dosage form | SOLUTION/ DROPS |
| Route | ORAL |
| Labeler | Guna spa |
| Product type | HUMAN OTC DRUG |
| Marketing category | UNAPPROVED HOMEOPATHIC |
| Pharmacologic classes | Allergens [CS], Cell-mediated Immunity [PE], Copper [CS], Copper-containing Intrauterine Device [EPC], Decreased Embryonic Implantation [PE], Decreased Sperm Motility [PE] and 6 more |
| Marketing start | May 27, 2010 |
| 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: