NDC product
GUNA DEEP CLEANSE
NDC 17089-466 · Guna spa
Key facts
| Product NDC | 17089-466 |
|---|---|
| Proprietary name | GUNA DEEP CLEANSE |
| Nonproprietary name | apis mellifera - berberis vulgaris root bark - chelidonium majus - chondrodendron tomentosum root - equisetum hyemale whole - fucus vesiculosus - galium aparine whole - hamamelis virginiana root bark… |
| Substances | CHELIDONIUM MAJUS ROOT, LYCOPODIUM CLAVATUM SPORE, SODIUM SULFATE, SOLIDAGO VIRGAUREA FLOWERING TOP, RANCID BEEF, FUCUS VESICULOSUS, GALIUM APARINE WHOLE, THUJA OCCIDENTALIS LEAFY TWIG, MYOSOTIS ARVENSIS, STRYCHNOS NUX-VOMICA SEED, PODOPHYLLUM PELTATUM ROOT, CHONDRODENDRON TOMENTOSUM ROOT and 4 more |
| Dosage form | SOLUTION/ DROPS |
| Route | ORAL |
| Labeler | Guna spa |
| Product type | HUMAN OTC DRUG |
| Marketing category | UNAPPROVED HOMEOPATHIC |
| Pharmacologic classes | Allergens [CS], Bee Venoms [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Increased Large Intestinal Motility [PE] and 7 more |
| Marketing start | Sep 24, 2020 |
| 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: