NDC 17089-291

GUNA-LYMPHO

Apis Mellifera - Calendula Officinalis Flower - Centella Asiatica - Dodecahydroxycyclohexane Dihydrate - Equisetum Hyemale - Fumaric Acid - Goldenseal - Graphite - Juglans Regia Leaf - Levothyroxine - Magnesium Phosphate - Malic Acid - Myosotis Arvensis - Phytolacca Americana Root - Sarsaparilla - Sodium Diethyl Oxalacetate - Sodium Pyruvate - Sus Scrofa Capillary Tissue - Sus Scrofa Small Intestine Mucosa Lymph Follicle - Sus Scrofa Vein - Taraxacum Officinale -

GUNA-LYMPHO is a Oral Solution/ Drops in the Human Otc Drug category. It is labeled and distributed by Guna Spa. The primary component is Apis Mellifera; Calendula Officinalis Flower; Sus Scrofa Capillary Tissue; Malic Acid; Equisetum Hyemale; Fumaric Acid; Graphite; Goldenseal; Centella Asiatica; Juglans Regia Leaf; Levothyroxine; Sus Scrofa Small Intestine Mucosa Lymph Follicle; Magnesium Phosphate, Tribasic, Pentahydrate; Myosotis Arvensis; Sodium Diethyl Oxalacetate; Sodium Pyruvate; Phytolacca Americana Root; Sarsaparilla; Taraxacum Officinale; Dodecahydroxycyclohexane Dihydrate; Sus Scrofa Vein.

Product ID17089-291_7d9f0a12-b0a5-75cd-e053-2a91aa0afec2
NDC17089-291
Product TypeHuman Otc Drug
Proprietary NameGUNA-LYMPHO
Generic NameApis Mellifera - Calendula Officinalis Flower - Centella Asiatica - Dodecahydroxycyclohexane Dihydrate - Equisetum Hyemale - Fumaric Acid - Goldenseal - Graphite - Juglans Regia Leaf - Levothyroxine - Magnesium Phosphate - Malic Acid - Myosotis Arvensis - Phytolacca Americana Root - Sarsaparilla - Sodium Diethyl Oxalacetate - Sodium Pyruvate - Sus Scrofa Capillary Tissue - Sus Scrofa Small Intestine Mucosa Lymph Follicle - Sus Scrofa Vein - Taraxacum Officinale -
Dosage FormSolution/ Drops
Route of AdministrationORAL
Marketing Start Date2006-05-23
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameGuna spa
Substance NameAPIS MELLIFERA; CALENDULA OFFICINALIS FLOWER; SUS SCROFA CAPILLARY TISSUE; MALIC ACID; EQUISETUM HYEMALE; FUMARIC ACID; GRAPHITE; GOLDENSEAL; CENTELLA ASIATICA; JUGLANS REGIA LEAF; LEVOTHYROXINE; SUS SCROFA SMALL INTESTINE MUCOSA LYMPH FOLLICLE; MAGNESIUM PHOSPHATE, TRIBASIC, PENTAHYDRATE; MYOSOTIS ARVENSIS; SODIUM DIETHYL OXALACETATE; SODIUM PYRUVATE; PHYTOLACCA AMERICANA ROOT; SARSAPARILLA; TARAXACUM OFFICINALE; DODECAHYDROXYCYCLOHEXANE DIHYDRATE; SUS SCROFA VEIN
Active Ingredient Strength8 [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL
NDC Exclude FlagN
Listing Certified Through2019-12-31

Packaging

NDC 17089-291-18

1 BOTTLE, DROPPER in 1 BOX (17089-291-18) > 30 mL in 1 BOTTLE, DROPPER
Marketing Start Date2018-12-21
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 17089-291-18 [17089029118]

GUNA-LYMPHO SOLUTION/ DROPS
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-12-21
Inactivation Date2020-01-31
Reactivation Date2020-03-13

Drug Details


© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.