NDC product
ANTI AGE SKIN
NDC 17089-046 · Guna spa
Key facts
| Product NDC | 17089-046 |
|---|---|
| Proprietary name | ANTI AGE SKIN |
| Nonproprietary name | alpha-tocopherol - ascophyllum nodosum - botryoglossum platycarpum - fucus serratus - fucus vesiculosus - isoleucine - leucine - retinol - selenium - sus scrofa capillary tissue - sus scrofa collagen… |
| Substances | ALPHA-TOCOPHEROL, LAMINARIA DIGITATA, BOTRYOGLOSSUM PLATYCARPUM, FUCUS SERRATUS, SUS SCROFA CAPILLARY TISSUE, UBIDECARENONE, SUS SCROFA COLLAGEN, FUCUS VESICULOSUS, ISOLEUCINE, ASCOPHYLLUM NODOSUM, LEUCINE, SUS SCROFA PLACENTA and 4 more |
| Dosage form | PELLET |
| Route | ORAL |
| Labeler | Guna spa |
| Product type | HUMAN OTC DRUG |
| Marketing category | UNAPPROVED HOMEOPATHIC |
| Pharmacologic classes | Allergens [CS], Cell-mediated Immunity [PE], Cells, Epidermal [EXT], Increased Histamine Release [PE], Increased IgG Production [PE] and 1 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: