Boost Remedy Water

Product NDC

35378-0002

11-digit product format

353780002

Labeler code

35378

Product ID

35378-0002_b46e9a34-442d-e4b4-6951-29d265e94951

Type

HUMAN OTC DRUG

Nonproprietary name

Adrenalinum, Aloe, Arsenicum alb., Baptisia, Berber. aqui., Berber. vulg., Bryonia, Chelidonium majus, Crotalus horridus, Digitalis, Ferrum metallicum, Glonoinum, Glycyrrhiza glabra, Hydrocotyle, Iodium, Iris versicolor, Lachesis, Lycopodium, Nat. mur., Nux vom., Rhus toxicodendron, Ruta, Thuja occ., Thyroidinum, Echinacea, Lappa, Solidago, Taraxacum

Dosage form

PELLET

Route

ORAL

Labeler

Georgetown Health, LLC DBA EssentiaLife

Marketing category

UNAPPROVED HOMEOPATHIC

Marketing start

2012-07-01

Marketing end

0000-00-00

Substance

EPINEPHRINE; ALOE; ARSENIC TRIOXIDE; BAPTISIA TINCTORIA ROOT; MAHONIA AQUIFOLIUM ROOT BARK; BERBERIS VULGARIS ROOT BARK; BRYONIA ALBA ROOT; CHELIDONIUM MAJUS; CROTALUS HORRIDUS HORRIDUS VENOM; DIGITALIS; IRON; NITROGLYCERIN; GLYCYRRHIZA GLABRA; CENTELLA ASIATICA; IODINE; IRIS VERSICOLOR ROOT; LACHESIS MUTA VENOM; LYCOPODIUM CLAVATUM SPORE; SODIUM CHLORIDE; STRYCHNOS NUX-VOMICA SEED; TOXICODENDRON PUBESCENS LEAF; RUTA GRAVEOLENS FLOWERING TOP; THUJA OCCIDENTALIS LEAFY TWIG; THYROID, UNSPECIFIED; ECHINACEA, UNSPECIFIED; ARCTIUM LAPPA ROOT; SOLIDAGO VIRGAUREA FLOWERING TOP; TARAXACUM OFFICINALE

Active strength

15 [hp_X]/mg; [hp_X]/mg; [hp_X]/mg; [hp_X]/mg; [hp_X]/mg; [hp_X]/mg; [hp_X]/mg; [hp_X]/mg; [hp_X]/mg; [hp_X]/mg; [hp_X]/mg; [hp_X]/mg; [hp_X]/mg; [hp_X]/mg; [hp_X]/mg; [hp_X]/mg; [hp_X]/mg; [hp_X]/mg; [hp_X]/mg; [hp_X]/mg; [hp_X]/mg; [hp_X]/mg; [hp_X]/mg; [hp_X]/mg; [hp_X]/mg; [hp_X]/mg; [hp_X]/mg; [hp_X]/mg

NDC exclude flag

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record