NDC product
GUNA SINUS PLUS
NDC 17089-472 · Guna spa
Key facts
| Product NDC | 17089-472 |
|---|---|
| Proprietary name | GUNA SINUS PLUS |
| Nonproprietary name | ALTHAEA OFFICINALIS LEAF - CALCIUM SULFIDE - COPPER - DRIMIA MARITIMA BULB - ECHINACEA ANGUSTIFOLIA - HYDRASTIS CANADENSIS WHOLE - LOBARIA PULMONARIA - MANGANESE - MERCURIC SULFIDE - ONION - PLANTAGO… |
| Substances | ONION, ALTHAEA OFFICINALIS LEAF, SILVER NITRATE, ASCORBIC ACID, HYDRASTIS CANADENSIS WHOLE, LOBARIA PULMONARIA, COPPER, ECHINACEA ANGUSTIFOLIA, CALCIUM SULFIDE, POTASSIUM DICHROMATE, MANGANESE, MERCURIC SULFIDE and 6 more |
| Dosage form | SPRAY |
| Route | NASAL |
| Labeler | Guna spa |
| Product type | HUMAN OTC DRUG |
| Marketing category | UNAPPROVED HOMEOPATHIC |
| Pharmacologic classes | Allergens [CS], Ascorbic Acid [CS], Cell-mediated Immunity [PE], Copper [CS], Copper-containing Intrauterine Device [EPC], Decreased Embryonic Implantation [PE] and 7 more |
| Marketing start | Feb 17, 2021 |
| 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: