- Product NDC
- 55138-013
- 11-digit product format
- 551380013
- Labeler code
- 55138
- Product ID
- 55138-013_0d9732a5-d779-4afa-bdeb-f2d261ab474b
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- american ginseng, arnica montana, turnera diffusa leafy twig, herring sperm DNA, galium aparine, hamamelis virginiana root bark/stem bark, pork liver, cervus elaphus horn oil, ovis aries testicle, phosphoric acid, sus scrofa pituitary gland, thuja occidentalis leafy twig, thyroid, unspecified, tribulus terrestris, ginger
- Dosage form
- SPRAY
- Route
- ORAL
- Labeler
- Integra Health International, S.A. de C.V.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2014-08-08
- Marketing end
- 0000-00-00
- Substance
- AMERICAN GINSENG; ARNICA MONTANA; TURNERA DIFFUSA LEAFY TWIG; HERRING SPERM DNA; GALIUM APARINE; HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK; PORK LIVER; CERVUS ELAPHUS HORN OIL; OVIS ARIES TESTICLE; PHOSPHORIC ACID; SUS SCROFA PITUITARY GLAND; THUJA OCCIDENTALIS LEAFY TWIG; THYROID, UNSPECIFIED; TRIBULUS TERRESTRIS; GINGER
- Active strength
- 2 [hp_C]/mg; [hp_C]/mg; [hp_C]/mg; [hp_C]/mg; [hp_C]/mg; [hp_C]/mg; [hp_C]/mg; [hp_C]/mg; [hp_C]/mg; [hp_C]/mg; [hp_C]/mg; [hp_C]/mg; [hp_C]/mg; [hp_C]/mg; [hp_C]/mg
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- Current FDA listing
- Historical FDA.report record