Home NDC 76472-3000 ACONITUM NAPELLUS
Product NDC 76472-3000
11-digit product format 764723000
Labeler code 76472
Product ID 76472-3000_0f3fe746-1484-0694-e063-6294a90a1583
Type HUMAN OTC DRUG
Nonproprietary name ACONITUM NAPELLUS
Dosage form PELLET
Route SUBLINGUAL
Labeler SEVENE USA
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2001-08-02
Substance ACONITUM NAPELLUS
Active strength 200 [kp_C]/1
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base ACONITUM NAPELLUS
Brand name suffix 200ck
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ACONITUM NAPELLUS 200 [kp_C]/1
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination U0NQ8555JD 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 76472-3000-1 ACONITUM NAPELLUS200ck 80 in 1 CYLINDER PELLET 80 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 76472-3000 ACONITUM NAPELLUS 200CK (ACONITUM NAPELLUS) PELLET [SEVENE USA] 3 Current NDC, Legacy NDC, 1 package rows 20240119_c89907e7-fa1c-9b1e-e053-2a95a90aac62.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 76472-3000-1 76472300001 80 PELLET in 1 CYLINDER (76472-3000-1) 80 pellet 2021-08-02 0000-00-00 No No Current