Robinia Nicotianna

Product NDC

48951-8394

11-digit product format

489518394

Labeler code

48951

Product ID

48951-8394_ea274431-c12e-e79c-e053-2995a90adbec

Type

HUMAN OTC DRUG

Nonproprietary name

Robinia Nicotiana

Dosage form

LIQUID

Route

ORAL

Labeler

Uriel Pharmacy, Inc.

Marketing category

UNAPPROVED HOMEOPATHIC

Marketing start

2009-09-01

Marketing end

0000-00-00

Substance

COPPER; ROBINIA PSEUDOACACIA BARK; SILVER; SODIUM PHOSPHATE; STRYCHNOS NUX-VOMICA SEED; SUS SCROFA ADRENAL GLAND; TOBACCO LEAF

Active strength

8 [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], Copper [CS], Copper-containing Intrauterine Device [EPC], Decreased Embryonic Implantation [PE], Decreased Sperm Motility [PE], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Increased IgG Production [PE], Inhibit Ovum Fertilization [PE], Non-Standardized Plant 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

2023-12-31

Current FDA listing

Historical FDA.report record