NDC product
GUNA-AWARENESS
NDC 17089-350 · Guna spa
Key facts
| Product NDC | 17089-350 |
|---|---|
| Proprietary name | GUNA-AWARENESS |
| Nonproprietary name | BETAINE - BUFO BUFO CUTANEOUS GLAND - CALCIUM CARBONATE - CHROMIC SULFATE - CICUTA VIROSA ROOT - COPPER - FOLIC ACID - GOLD - COBALAMIN - IRON - LACHESIS MUTA VENOM - MELATONIN - MOLYBDENUM… |
| Substances | LACHESIS MUTA VENOM, MELATONIN, MOLYBDENUM, NEUROTROPHIN-3, NEUROTROPHIN-4, OXYTOCIN, SILICON DIOXIDE, SUS SCROFA TEMPORAL LOBE, THYROTROPIN ALFA, BETAINE, VANADIUM, ZINC and 12 more |
| Dosage form | SOLUTION/ DROPS |
| Route | ORAL |
| Labeler | Guna spa |
| Product type | HUMAN OTC DRUG |
| Marketing category | UNAPPROVED HOMEOPATHIC |
| Pharmacologic classes | Allergens [CS], Blood Coagulation Factor [EPC], Calcium [CS], Cations, Divalent [CS], Cell-mediated Immunity [PE] and 17 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: