Prime

Product NDC

55714-2552

11-digit product format

557142552

Labeler code

55714

Product ID

55714-2552_2dd1e42d-6f1d-a6fb-e063-6294a90ad8d7

Type

HUMAN OTC DRUG

Nonproprietary name

Ginkgo biloba, Ruta graveolens, Agnus castus, Allium sativum, Ambra grisea, Angelica sinensis radix, Aralia quinquefolia, Arnica montana, Arsenicum album, Avena sativa, Baptisia tinctoria, Baryta carbonica, Bryonia, Cantharis, Lachesis mutus, Lycopodium clavatum, Nux vomica, Phosphoricum acidum, Pulsatilla, Ruta graveolens, Sabal serrulata, Selenium metallicum, Zincum metallicum.

Dosage form

LIQUID

Route

ORAL

Labeler

Newton Laboratories, Inc.

Marketing category

UNAPPROVED HOMEOPATHIC

Marketing start

2019-08-01

Substance

AMBERGRIS; AMERICAN GINSENG; ANEMONE PULSATILLA; ANGELICA SINENSIS ROOT; ARNICA MONTANA; ARSENIC TRIOXIDE; AVENA SATIVA FLOWERING TOP; BAPTISIA TINCTORIA ROOT; BARIUM CARBONATE; BRYONIA ALBA ROOT; CHASTE TREE FRUIT; GARLIC; GINKGO; LACHESIS MUTA VENOM; LYCOPODIUM CLAVATUM SPORE; LYTTA VESICATORIA; PHOSPHORIC ACID; RUTA GRAVEOLENS FLOWERING TOP; SAW PALMETTO; SELENIUM; STRYCHNOS NUX-VOMICA SEED; ZINC

Active strength

15; 15; 15; 15; 15; 15; 15; 15; 15; 15; 15; 15; 6; 15; 15; 15; 15; 15; 15; 15; 15; 15 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL

Pharmacologic classes

Allergens [CS], Allergens [CS], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Dietary Proteins [CS], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Non-Standardized Food Allergenic Extract [EPC], Non-Standardized Plant Allergenic Extract [EPC], Plant Proteins [CS], Plant Proteins [CS], Seed Storage Proteins [CS]

NDC exclude flag

No

Listing certified through

2026-12-31

Current FDA listing

Yes