Home NDC 57556-017 Pulsatilla
Product NDC 57556-017
11-digit product format 575560017
Labeler code 57556
Product ID 57556-017_40941606-17ac-43f2-e063-6394a90acbc2
Type HUMAN OTC DRUG
Nonproprietary name Pulsatilla
Dosage form PELLET
Route ORAL
Labeler Historical Remedies
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2021-07-06
Substance ANEMONE PULSATILLA
Active strength 12 [hp_X]/g
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base Pulsatilla
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ANEMONE PULSATILLA 12 [hp_X]/g
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.
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 57556-017-02 Pulsatilla 14 g in 1 BOTTLE, GLASS PELLET 14 9
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 57556-017 PULSATILLA PELLET [HISTORICAL REMEDIES] 8 Current NDC, Legacy NDC, 1 package rows 20241105_c6790a91-d601-8c37-e053-2995a90a0a0c.zip
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 Marketing end Sample Exclude flag Status 57556-017-02 57556001702 14 g in 1 BOTTLE, GLASS (57556-017-02) 14 g 2021-07-06 0000-00-00 No No Current