NDC product
GUNA-REFLUX
NDC 17089-406 · Guna spa
Key facts
| Product NDC | 17089-406 |
|---|---|
| Proprietary name | GUNA-REFLUX |
| Nonproprietary name | ACTIVATED CHARCOAL - AETHUSA CYNAPIUM - APOMORPHINE HYDROCHLORIDE - BRYONIA ALBA ROOT - COLCHICUM AUTUMNALE BULB - IPECAC - LYCOPODIUM CLAVATUM SPORE - STRYCHNOS IGNATII SEED - STRYCHNOS NUX-VOMICA… |
| Substances | AETHUSA CYNAPIUM, APOMORPHINE HYDROCHLORIDE, BRYONIA ALBA ROOT, ACTIVATED CHARCOAL, SUS SCROFA STOMACH, COLCHICUM AUTUMNALE BULB, WATERMELON, SUS SCROFA ESOPHAGUS, STRYCHNOS IGNATII SEED, IPECAC, LYCOPODIUM CLAVATUM SPORE, STRYCHNOS NUX-VOMICA SEED |
| Dosage form | SOLUTION/ DROPS |
| Route | ORAL |
| Labeler | Guna spa |
| Product type | HUMAN OTC DRUG |
| Marketing category | UNAPPROVED HOMEOPATHIC |
| Pharmacologic classes | Allergens [CS], Cell-mediated Immunity [PE], Dietary Proteins [CS], Dopamine Agonists [MoA], Dopaminergic Agonist [EPC], Fruit Proteins [EXT] and 6 more |
| Marketing start | May 12, 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: