NDC product
GUNA-FLAM
NDC 17089-417 · Guna spa
Key facts
| Product NDC | 17089-417 |
|---|---|
| Proprietary name | GUNA-FLAM |
| Nonproprietary name | ACONITUM NAPELLUS - APIS MELLIFERA - ATROPA BELLADONNA - BASIC CUPRIC CARBONATE - BRYONIA ALBA ROOT - CALCIUM SULFIDE - CITRIC ACID MONOHYDRATE - FERRIC PHOSPHATE - INTERLEUKIN-10 - MELATONIN… |
| Substances | ACONITUM NAPELLUS, ANTI-INTERLEUKIN-1.ALPHA. IMMUNOGLOBULIN G RABBIT, APIS MELLIFERA, ATROPA BELLADONNA, METENKEFALIN, BRYONIA ALBA ROOT, CITRIC ACID MONOHYDRATE, SUS SCROFA CONJUNCTIVA, BASIC CUPRIC CARBONATE, FERRIC PHOSPHATE, CALCIUM SULFIDE, SUS SCROFA PITUITARY GLAND and 7 more |
| Dosage form | SOLUTION/ DROPS |
| Route | ORAL |
| Labeler | Guna spa |
| Product type | HUMAN OTC DRUG |
| Marketing category | UNAPPROVED HOMEOPATHIC |
| Pharmacologic classes | Acidifying Activity [MoA], Allergens [CS], Anti-coagulant [EPC], Bee Venoms [CS], Calcium Chelating Activity [MoA], Calculi Dissolution Agent [EPC] and 9 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: