NDC product
GUNA-CELL
NDC 17089-450 · Guna spa
Key facts
| Product NDC | 17089-450 |
|---|---|
| Proprietary name | GUNA-CELL |
| Nonproprietary name | acetylcarnitine, l-ampc-alpha-lipoic ac-a-tocopherol-ascorbic acid-calc carb-citric ac-cobalamin-colchicum-conium-cupric sulf-herring sperm dna-ferrous fumarate-folic acid-fumaric acid-kali aspartate-mang phos-mang… |
| Substances | ACETYLCARNITINE, ADENOSINE CYCLIC PHOSPHATE, .ALPHA.-LIPOIC ACID, .ALPHA.-TOCOPHEROL ACETATE, DL-, ASCORBIC ACID, CALCIUM CARBONATE, CITRIC ACID MONOHYDRATE, COBALAMIN, COLCHICUM AUTUMNALE BULB, CONIUM MACULATUM FLOWERING TOP, CUPRIC SULFATE, HERRING SPERM DNA and 22 more |
| Dosage form | SOLUTION/ DROPS |
| Route | ORAL |
| Labeler | Guna spa |
| Product type | HUMAN OTC DRUG |
| Marketing category | UNAPPROVED HOMEOPATHIC |
| Pharmacologic classes | Acidifying Activity [MoA], Analogs/Derivatives [Chemical/Ingredient], Anti-coagulant [EPC], Ascorbic Acid [CS], Blood Coagulation Factor [EPC], Calcium Chelating Activity [MoA] and 24 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: