NDC product
GUNA-MOOD
NDC 17089-265 · Guna spa
Key facts
| Product NDC | 17089-265 |
|---|---|
| Proprietary name | GUNA-MOOD |
| Nonproprietary name | 5-hydroxy tryptophan, dl - alfalfa - avena sativa flowering top - lachesis muta venom - phosphoric acid - salix alba bark - salmonella enterica subsp. enterica serovar typhi - sepia officinalis juice - serotonin… |
| Substances | 5-HYDROXYTRYPTOPHAN, DL-, ALFALFA, AVENA SATIVA FLOWERING TOP, STRYCHNOS IGNATII SEED, LACHESIS MUTA VENOM, PHOSPHORIC ACID, SUS SCROFA PINEAL GLAND, SALIX ALBA BARK, SALMONELLA ENTERICA SUBSP. ENTERICA SEROVAR TYPHI, SEPIA OFFICINALIS JUICE, SEROTONIN, SUS SCROFA THYMUS and 1 more |
| Dosage form | SOLUTION/ DROPS |
| Route | ORAL |
| Labeler | Guna spa |
| Product type | HUMAN OTC DRUG |
| Marketing category | UNAPPROVED HOMEOPATHIC |
| 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: