NDC product

OMEOSPORT

NDC 17089-075 · Guna spa

Key facts

Product NDC 17089-075
Proprietary name OMEOSPORT
Nonproprietary name .ALPHA.-KETOGLUTARIC ACID - ACONITIC ACID, CIS - ADENOSINE TRIPHOSPHATE - ALPHA LIPOIC ACID - ASCORBIC ACID - ASIAN GINSENG - BARIUM CATION - BEET - CEROUS OXALATE NONAHYDRATE - COENZYME A - CYSTEINE - FUMARIC ACID - LACTIC ACID, DL - MAGNESIUM CARBONATE - MALIC ACID - MANGANESE PHOSPHATE, DIBASIC - PORK - PYRIDOXINE HYDROCHLORIDE - RIBOFLAVIN - SODIUM DIETHYL OXALACETATE - SODIUM PYRUVATE - SUCCINIC ACID - SUS SCROFA ADRENAL GLAND - THIAMINE HYDROCHLORIDE - SUS SCROFA EMBRYO -
Substances ADENOSINE TRIPHOSPHATE, .ALPHA.-KETOGLUTARIC ACID, .ALPHA.-LIPOIC ACID, ASCORBIC ACID, BARIUM OXALOSUCCINATE, BEET, CEROUS OXALATE NONAHYDRATE, ACONITIC ACID, (Z)-, COENZYME A, CYSTEINE, SUS SCROFA EMBRYO, FUMARIC ACID and 13 more
Dosage form PELLET
Route ORAL
Labeler Guna spa
Product type HUMAN OTC DRUG
Marketing category UNAPPROVED HOMEOPATHIC
Pharmacologic classes Allergens [CS], Analogs/Derivatives [Chemical/Ingredient], Ascorbic Acid [CS], Cell-mediated Immunity [PE], Dietary Proteins [CS], Increased Histamine Release [PE] and 10 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:

Browse all National Drug Codes (NDC)