Robinia Nicotiana

Product NDC
48951-8374
11-digit product format
489518374
Labeler code
48951
Product ID
48951-8374_c364e01a-5e57-509e-e053-2a95a90a3c89
Type
HUMAN OTC DRUG
Nonproprietary name
Robinia Nicotiana
Dosage form
PELLET
Route
ORAL
Labeler
Uriel Pharmacy Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2009-09-01
Marketing end
0000-00-00
Substance
ROBINIA PSEUDOACACIA BARK; SILVER; SUS SCROFA ADRENAL GLAND; TOBACCO LEAF; STRYCHNOS NUX-VOMICA SEED; COPPER; SODIUM PHOSPHATE
Active strength
4 [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1
NDC exclude flag
No
Listing certified through
2022-12-31
Current FDA listing
Historical FDA.report record

Related Records

Related UNII Ingredients

UNIIPreferred termRegistry numberMatched term
7TPC058OWYROBINIA PSEUDOACACIA BARKROBINIA PSEUDOACACIA BARK
3M4G523W1GSILVER7440-22-4SILVER
398IYQ16YVSUS SCROFA ADRENAL GLANDSUS SCROFA ADRENAL GLAND
6YR2608RSUTOBACCO LEAF8037-19-2TOBACCO LEAF
269XH13919STRYCHNOS NUX-VOMICA SEED8046-97-7STRYCHNOS NUX-VOMICA SEED
789U1901C5COPPER7440-50-8COPPER
SE337SVY37SODIUM PHOSPHATE7632-05-5SODIUM PHOSPHATE

Packages

Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
48951-8374-2489518374021350 PELLET in 1 BOTTLE, GLASS (48951-8374-2) 1350 pellet2009-09-010000-00-00NoNoCurrent

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Robinia NicotianaUriel Pharmacy Inc.2021-05-27HUMAN OTC DRUG LABEL1