- Product NDC
- 48951-8397
- 11-digit product format
- 489518397
- Labeler code
- 48951
- Product ID
- 48951-8397_eaed2e4b-d6c0-2e8d-e053-2995a90a1985
- 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
- BOS TAURUS ADRENAL GLAND; COPPER; ROBINIA PSEUDOACACIA BARK; SILVER; SODIUM PHOSPHATE; STRYCHNOS NUX-VOMICA SEED; 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