Home NDC 60986-2035 ABC
Product NDC 60986-2035
11-digit product format 609862035
Labeler code 60986
Product ID 60986-2035_483b7f10-381e-7b69-e063-6394a90a621f
Type HUMAN OTC DRUG
Nonproprietary name ACONITUM NAPELLUS, BELLADONNA, CHAMOMILLA
Dosage form LIQUID
Route ORAL
Labeler MARCO PHARMA INTERNATIONAL LLC
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2015-01-22
Substance ACONITUM NAPELLUS; BELLADONNA LEAF; MATRICARIA RECUTITA
Active strength 3; 3; 3 [hp_X]/100mL; [hp_X]/100mL; [hp_X]/100mL
NDC exclude flag No
Listing certified through 2027-12-31
Current FDA listing Yes Observed NDC auxiliary status history# This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
Historic NDC status page 1 of 1 · 15 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Package NDC Code Status Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 excluded package package 60986-2035-5 D Discontinued by firm d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 excluded package package 60986-2035-5 D Discontinued by firm f5e01cc5f278…a2eaf40c39c3…2025-04-01 02:39 UTC · source 2025-03-31 excluded package package 60986-2035-5 D Discontinued by firm 2ef7874e63bc…57b86245f4fa…2025-03-28 20:22 UTC · source 2025-03-28 excluded package package 60986-2035-5 D Discontinued by firm a1b67e2a42f9…c4cf2c586c0d…2025-03-22 03:12 UTC · source 2025-03-21 excluded package package 60986-2035-5 D Discontinued by firm cfe11265f3b6…090c488252e2…2025-03-10 12:48 UTC · source 2025-03-10 excluded package package 60986-2035-5 D Discontinued by firm cdf11ea48f46…ba0047e9e063…2025-02-02 03:52 UTC · source 2025-01-31 excluded package package 60986-2035-5 D Discontinued by firm 302b2466d912…e7b80fea0513…2025-01-20 13:05 UTC · source 2025-01-20 excluded package package 60986-2035-5 D Discontinued by firm ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 excluded package package 60986-2035-5 D Discontinued by firm 0efc9e666f02…f202fb6c5f17…2020-12-18 03:04 UTC · source 2020-12-17 excluded product product I Inactivated by FDA e2bbac7714bc…27bdfed8d636…2020-12-18 03:04 UTC · source 2020-12-17 excluded package package 60986-2035-5 I Inactivated by FDA e2bbac7714bc…27bdfed8d636…2020-06-10 20:45 UTC · source 2020-06-10 excluded product product I Inactivated by FDA 9bebd1f3094a…5416666fcb17…2020-06-10 20:45 UTC · source 2020-06-10 excluded package package 60986-2035-5 I Inactivated by FDA 9bebd1f3094a…5416666fcb17…2019-12-08 06:16 UTC · source 2019-12-05 excluded product product E Excluded after deficient or non-compliant submission was not corrected 110d247fa046…a55b01930146…2019-12-08 06:16 UTC · source 2019-12-05 excluded package package 60986-2035-5 E Excluded after deficient or non-compliant submission was not corrected 110d247fa046…a55b01930146…
Additional Listing Data#
Finished product Yes
Brand name base ABC
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ACONITUM NAPELLUS 3 [hp_X]/100mL MATRICARIA RECUTITA 3 [hp_X]/100mL BELLADONNA LEAF 3 [hp_X]/100mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 3 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination U0NQ8555JD Internal UNII lookup G0R4UBI2ZZ Internal UNII lookup 6GZW20TIOI Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 60986-2035-3 ABC 50 mL in 1 BOTTLE, DROPPER LIQUID 50 5 60986-2035-5 ABC 20 mL in 1 BOTTLE LIQUID 20 5
DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded ACONITUM NAPELLUS ACTIVE INGREDIENT U0NQ8555JD ABC (ACONITUM NAPELLUS, BELLADONNA, CHAMOMILLA) LIQUID [MARCO PHARMA INTERNATIONAL LLC] 1 BELLADONNA LEAF ACTIVE INGREDIENT 6GZW20TIOI ABC (ACONITUM NAPELLUS, BELLADONNA, CHAMOMILLA) LIQUID [MARCO PHARMA INTERNATIONAL LLC] 1 MATRICARIA RECUTITA ACTIVE INGREDIENT G0R4UBI2ZZ ABC (ACONITUM NAPELLUS, BELLADONNA, CHAMOMILLA) LIQUID [MARCO PHARMA INTERNATIONAL LLC] 1 ACONITUM NAPELLUS ACTIVE MOIETY U0NQ8555JD ABC (ACONITUM NAPELLUS, BELLADONNA, CHAMOMILLA) LIQUID [MARCO PHARMA INTERNATIONAL LLC] 1 BELLADONNA LEAF ACTIVE MOIETY 6GZW20TIOI ABC (ACONITUM NAPELLUS, BELLADONNA, CHAMOMILLA) LIQUID [MARCO PHARMA INTERNATIONAL LLC] 1 MATRICARIA RECUTITA ACTIVE MOIETY G0R4UBI2ZZ ABC (ACONITUM NAPELLUS, BELLADONNA, CHAMOMILLA) LIQUID [MARCO PHARMA INTERNATIONAL LLC] 1 ALCOHOL INACTIVE INGREDIENT 3K9958V90M ABC (ACONITUM NAPELLUS, BELLADONNA, CHAMOMILLA) LIQUID [MARCO PHARMA INTERNATIONAL LLC] 1 WATER INACTIVE INGREDIENT 059QF0KO0R ABC (ACONITUM NAPELLUS, BELLADONNA, CHAMOMILLA) LIQUID [MARCO PHARMA INTERNATIONAL LLC] 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 60986-2035 ABC (ACONITUM NAPELLUS, BELLADONNA, CHAMOMILLA) LIQUID [MARCO PHARMA INTERNATIONAL LLC] 4 Current NDC, Legacy NDC, 2 package rows 20241207_44749e04-ca70-410d-a754-8befe8da11e7.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.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join ABC ACONITUM NAPELLUS, BELLADONNA, CHAMOMILLA MARCO PHARMA INTERNATIONAL LLC 44749e04-ca70-410d-a754-8befe8da11e7 2026-01-12 Warnings Exact identifier ndc (product): 60986-2035
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 60986-2035-3 60986203503 50 mL in 1 BOTTLE, DROPPER (60986-2035-3) 50 ml 2024-12-03 No No Current 60986-2035-5 60986203505 20 mL in 1 BOTTLE (60986-2035-5) 20 ml 2015-01-27 0000-00-00 No No Current