NDC 17089-237

GUNA-REACT

Angelica Sinensis Root - Arnica Montana - Asian Ginseng - Echinacea Angustifolia - Fomitopsis Pinicola Fruiting Body - Interferon Gamma-1b - Paeonia Officinalis Root - Pork Liver - Reishi - Silybum Marianum Seed - Sus Scrofa Small Intestine Mucosa Lymph Follicle - Turmeric -

GUNA-REACT is a Oral Pellet in the Human Otc Drug category. It is labeled and distributed by Guna Spa. The primary component is Turmeric; Angelica Sinensis Root; Arnica Montana; Silybum Marianum Seed; Echinacea Angustifolia; Asian Ginseng; Pork Liver; Interferon Gamma-1b; Reishi; Sus Scrofa Small Intestine Mucosa Lymph Follicle; Paeonia Officinalis Root; Fomitopsis Pinicola Fruiting Body.

Product ID17089-237_7e7d6ebc-5974-b9fc-e053-2991aa0a2ae5
NDC17089-237
Product TypeHuman Otc Drug
Proprietary NameGUNA-REACT
Generic NameAngelica Sinensis Root - Arnica Montana - Asian Ginseng - Echinacea Angustifolia - Fomitopsis Pinicola Fruiting Body - Interferon Gamma-1b - Paeonia Officinalis Root - Pork Liver - Reishi - Silybum Marianum Seed - Sus Scrofa Small Intestine Mucosa Lymph Follicle - Turmeric -
Dosage FormPellet
Route of AdministrationORAL
Marketing Start Date2006-05-23
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameGuna spa
Substance NameTURMERIC; ANGELICA SINENSIS ROOT; ARNICA MONTANA; SILYBUM MARIANUM SEED; ECHINACEA ANGUSTIFOLIA; ASIAN GINSENG; PORK LIVER; INTERFERON GAMMA-1B; REISHI; SUS SCROFA SMALL INTESTINE MUCOSA LYMPH FOLLICLE; PAEONIA OFFICINALIS ROOT; FOMITOPSIS PINICOLA FRUITING BODY
Active Ingredient Strength3 [hp_X]/4g; [hp_X]/4g; [hp_X]/4g; [hp_X]/4g; [hp_X]/4g; [hp_X]/4g; [hp_C]/4g; [hp_C]/4g; [hp_X]/4g; [hp_C]/4g; [hp_X]/4g; [hp_X]/4g
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 17089-237-20

2 TUBE in 1 BOX (17089-237-20) > 4 g in 1 TUBE
Marketing Start Date2018-12-21
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 17089-237-20 [17089023720]

GUNA-REACT PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-12-21

Drug Details

Active Ingredients

IngredientStrength
TURMERIC3 [hp_X]/4g

OpenFDA Data

SPL SET ID:c2b64907-1ae2-4686-b13c-847dbb84724e
Manufacturer
UNII
UPC Code
  • 0317089237204

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