NDC product
GUNA-HEMORRHOIDS
NDC 17089-296 · Guna spa
Key facts
| Product NDC | 17089-296 |
|---|---|
| Proprietary name | GUNA-HEMORRHOIDS |
| Nonproprietary name | activated charcoal - arnica montana - atropa belladonna - canakinumab - hydrocotyle asiatica extract - aesculus hippocastanum flower - melissa officinalis - paeonia officinalis root - podophyllum… |
| Substances | AESCULUS HIPPOCASTANUM FLOWER, ANTI-INTERLEUKIN-1.ALPHA. IMMUNOGLOBULIN G RABBIT, CANAKINUMAB, ARNICA MONTANA, ATROPA BELLADONNA, ACTIVATED CHARCOAL, HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK, PORK LIVER, HYDROCOTYLE ASIATICA EXTRACT, SUS SCROFA SMALL INTESTINE MUCOSA LYMPH FOLLICLE, MELISSA OFFICINALIS, STRYCHNOS NUX-VOMICA SEED and 3 more |
| 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], Increased Histamine Release [PE], Increased IgG Production [PE], Non-Standardized Plant Allergenic Extract [EPC], Plant Proteins [CS] and 1 more |
| Marketing start | Apr 16, 2008 |
| 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: