Home NDC 53645-1983-6 Pulsatilla 6X
Product NDC 53645-1983
Requested package NDC 53645-1983-6
11-digit product format 536451983
Labeler code 53645
Product ID 53645-1983_3dead232-3111-e085-e063-6294a90a0926
Type HUMAN OTC DRUG
Nonproprietary name PULSATILLA VULGARIS
Dosage form LIQUID
Route ORAL
Labeler True Botanica, LLC
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2026-07-21
Substance PULSATILLA VULGARIS
Active strength 6 [hp_X]/30mL
Listing certified through 2027-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base Pulsatilla 6X
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength PULSATILLA VULGARIS 6 [hp_X]/30mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination I76KB35JEV 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 Status 53645-1983-6 53645198306 30 mL in 1 BOTTLE (53645-1983-6) 30 ml 2026-07-21 0 Current