NDC product
GUNA-DIZZY
NDC 17089-306 · Guna spa
Key facts
| Product NDC | 17089-306 |
|---|---|
| Proprietary name | GUNA-DIZZY |
| Nonproprietary name | .alpha.-ketoglutaric acid - ambergris - anamirta cocculus seed - conium maculatum flowering top - epinephrine - fumaric acid - malic acid - melatonin - mineral oil - pteridium aquilinum root… |
| Substances | EPINEPHRINE, .ALPHA.-KETOGLUTARIC ACID, AMBERGRIS, SUS SCROFA ARTERY, SUS SCROFA CEREBELLUM, QUININE SALICYLATE, ANAMIRTA COCCULUS SEED, CONIUM MACULATUM FLOWERING TOP, FUMARIC ACID, MALIC ACID, MELATONIN, MINERAL OIL and 6 more |
| Dosage form | SOLUTION/ DROPS |
| Route | ORAL |
| Labeler | Guna spa |
| Product type | HUMAN OTC DRUG |
| Marketing category | UNAPPROVED HOMEOPATHIC |
| Pharmacologic classes | Adrenergic alpha-Agonists [MoA], Adrenergic beta-Agonists [MoA], Allergens [CS], Analogs/Derivatives [Chemical/Ingredient], Antimalarial [EPC], Catecholamine [EPC] and 13 more |
| Marketing start | May 23, 2006 |
| 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: