GUNA FLAM RELIEF

Product NDC

17089-464

11-digit product format

170890464

Labeler code

17089

Product ID

17089-464_af5aec5c-a562-6516-e053-2a95a90a3be9

Type

HUMAN OTC DRUG

Nonproprietary name

ACONITUM NAPELLUS - APIS MELLIFERA - ARNICA MONTANA WHOLE - ATROPA BELLADONNA - BASIC CUPRIC CARBONATE - BRYONIA ALBA ROOT - MATRICARIA CHAMOMILLA WHOLE - CALCIUM SULFIDE - CITRIC ACID MONOHYDRATE - ECHINACEA ANGUSTIFOLIA - FERRIC PHOSPHATE - PHYTOLACCA AMERICANA ROOT - RANCID BEEF - SODIUM PYRUVATE - PORK LIVER - RANCID BEEF - SUS SCROFA PITUITARY GLAND -

Dosage form

SOLUTION/ DROPS

Route

ORAL

Labeler

Guna spa

Marketing category

UNAPPROVED HOMEOPATHIC

Marketing start

2020-09-24

Substance

ACONITUM NAPELLUS WHOLE; APIS MELLIFERA; ARNICA MONTANA; ATROPA BELLADONNA; BASIC CUPRIC CARBONATE; BRYONIA ALBA ROOT; CALCIUM SULFIDE; CITRIC ACID MONOHYDRATE; ECHINACEA ANGUSTIFOLIA WHOLE; FERRIC PHOSPHATE; MATRICARIA CHAMOMILLA WHOLE; PHYTOLACCA AMERICANA ROOT; PORK LIVER; RANCID BEEF; SODIUM PYRUVATE; SUS SCROFA PITUITARY GLAND

Active strength

6; 6; 3; 6; 4; 6; 6; 3; 4; 12; 2; 6; 6; 30; 3; 200 [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

Pharmacologic classes

Acidifying Activity [MoA], Allergens [CS], Anti-coagulant [EPC], Bee Venoms [CS], Calcium Chelating Activity [MoA], Calculi Dissolution Agent [EPC], Cell-mediated Immunity [PE], Decreased Coagulation Factor Activity [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Iron [CS], Parenteral Iron Replacement [EPC], Phosphate Binder [EPC], Phosphate Chelating Activity [MoA], Standardized Insect Venom Allergenic Extract [EPC]

NDC exclude flag

No

Listing certified through

2026-12-31

Current FDA listing

Yes