Home NDC 53645-2630 Aurum Pentas
Product NDC 53645-2630
11-digit product format 536452630
Labeler code 53645
Product ID 53645-2630_561c2e0e-e3b8-9b21-e063-6294a90a2ad6
Type HUMAN OTC DRUG
Nonproprietary name Aurum Metallicum 7X, 11X, 18X, 30X
Dosage form LIQUID
Route ORAL
Labeler True Botanica, LLC
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2026-07-08
Substance GOLD
Active strength 7 [hp_X]/30mL
Pharmacologic classes Allergens [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Standardized Chemical Allergen [EPC]
NDC exclude flag No
Listing certified through 2027-12-31
Current FDA listing Yes Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base Aurum Pentas
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength GOLD 7 [hp_X]/30mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 79Y1949PYO Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 1 of 1 · 1 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 53645-2630-6 53645263006 30 mL in 1 BOTTLE (53645-2630-6) 30 ml 2026-07-08 No No Current