NDC product
GUNA-GERIATRICS
NDC 17089-349 · Guna spa
Key facts
| Product NDC | 17089-349 |
|---|---|
| Proprietary name | GUNA-GERIATRICS |
| Nonproprietary name | 1, 4-benzoquinone - arnica montana - oxytocin - barium carbonate - barium oxalosuccinate - corticotropin - lead - levothyroxine - lutrelin - malic acid - melatonin - neurotrophin-3 - neurotrophin-4… |
| Substances | QUINONE, BARIUM OXALOSUCCINATE, CORTICOTROPIN, ARNICA MONTANA, BARIUM CARBONATE, BRAIN-DERIVED NEUROTROPHIC FACTOR HUMAN, MALIC ACID, SUS SCROFA FRONTAL LOBE, SUS SCROFA ADRENAL GLAND, PORK LIVER, SUS SCROFA HYPOTHALAMUS, RINFABATE and 10 more |
| Dosage form | SOLUTION/ DROPS |
| Route | ORAL |
| Labeler | Guna spa |
| Product type | HUMAN OTC DRUG |
| Marketing category | UNAPPROVED HOMEOPATHIC |
| Pharmacologic classes | Adrenocorticotropic Hormone [CS], Adrenocorticotropic Hormone [EPC], Increased Uterine Smooth Muscle Contraction or Tone [PE], Oxytocic [EPC], Oxytocin [CS], Thyroid Stimulating Hormone [EPC] and 3 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: