Argentite Urtica

Product NDC
48951-1073
11-digit product format
489511073
Labeler code
48951
Product ID
48951-1073_69faffab-c128-e4b6-e053-2a91aa0a3571
Type
HUMAN OTC DRUG
Nonproprietary name
Argentite Urtica
Dosage form
LIQUID
Route
ORAL
Labeler
Uriel Pharmacy Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2009-09-01
Marketing end
0000-00-00
Substance
SAW PALMETTO; URTICA DIOICA; ROYAL JELLY; SILVER SULFIDE; BOS TAURUS PITUITARY GLAND; BOS TAURUS TESTICLE
Active strength
4 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
NDC exclude flag
No
Listing certified through
2020-12-31
Current FDA listing
Historical FDA.report record

Related Records

Related UNII Ingredients

UNIIPreferred termRegistry numberMatched term
J7WWH9M8QSSAW PALMETTOSAW PALMETTO
710FLW4U46URTICA DIOICAURTICA DIOICA
L497I37F0CROYAL JELLY8031-67-2ROYAL JELLY
9ZB10YHC1CSILVER SULFIDE21548-73-2SILVER SULFIDE
PR4RXL6G2HBOS TAURUS TESTICLEBOS TAURUS TESTICLE

Packages

Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
48951-1073-34895110730360 mL in 1 BOTTLE, DROPPER (48951-1073-3) 60 ml2009-09-010000-00-00NoNoCurrent