Home NDC 60986-2030 ABB
Product NDC 60986-2030
11-digit product format 609862030
Labeler code 60986
Product ID 60986-2030_d2bcc010-0beb-afe7-e053-2a95a90a4a0b
Type HUMAN OTC DRUG
Nonproprietary name ACONITUM NAPELLUS, BRYONIA ALBA, BELLADONNA
Dosage form LIQUID
Route ORAL
Labeler MARCO PHARMA INTERNATIONAL LLC
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2015-01-22
Marketing end 0000-00-00
Substance ACONITUM NAPELLUS; BRYONIA ALBA WHOLE; BELLADONNA LEAF
Active strength 3 [hp_X]/100mL; [hp_X]/100mL; [hp_X]/100mL
NDC exclude flag No
Listing certified through 2022-12-31
Current FDA listing Historical FDA.report record 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 · 6 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 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 60986-2030-5 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 60986-2030-5 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 60986-2030-5 E Excluded after deficient or non-compliant submission was not corrected 110d247fa046…a55b01930146…
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 60986-2030-5 ABB 20 mL in 1 BOTTLE LIQUID 20 3
DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded ACONITUM NAPELLUS ACTIVE INGREDIENT U0NQ8555JD ABB (ACONITUM NAPELLUS, BRYONIA ALBA, BELLADONNA) LIQUID [MARCO PHARMA INTERNATIONAL LLC] 1 BELLADONNA LEAF ACTIVE INGREDIENT 6GZW20TIOI ABB (ACONITUM NAPELLUS, BRYONIA ALBA, BELLADONNA) LIQUID [MARCO PHARMA INTERNATIONAL LLC] 1 BRYONIA ALBA WHOLE ACTIVE INGREDIENT 56K0VVT47P ABB (ACONITUM NAPELLUS, BRYONIA ALBA, BELLADONNA) LIQUID [MARCO PHARMA INTERNATIONAL LLC] 1 ACONITUM NAPELLUS ACTIVE MOIETY U0NQ8555JD ABB (ACONITUM NAPELLUS, BRYONIA ALBA, BELLADONNA) LIQUID [MARCO PHARMA INTERNATIONAL LLC] 1 BELLADONNA LEAF ACTIVE MOIETY 6GZW20TIOI ABB (ACONITUM NAPELLUS, BRYONIA ALBA, BELLADONNA) LIQUID [MARCO PHARMA INTERNATIONAL LLC] 1 BRYONIA ALBA WHOLE ACTIVE MOIETY 56K0VVT47P ABB (ACONITUM NAPELLUS, BRYONIA ALBA, BELLADONNA) LIQUID [MARCO PHARMA INTERNATIONAL LLC] 1 ALCOHOL INACTIVE INGREDIENT 3K9958V90M ABB (ACONITUM NAPELLUS, BRYONIA ALBA, BELLADONNA) LIQUID [MARCO PHARMA INTERNATIONAL LLC] 1 WATER INACTIVE INGREDIENT 059QF0KO0R ABB (ACONITUM NAPELLUS, BRYONIA ALBA, BELLADONNA) LIQUID [MARCO PHARMA INTERNATIONAL LLC] 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 60986-2030 ABB (ACONITUM NAPELLUS, BRYONIA ALBA, BELLADONNA) LIQUID [MARCO PHARMA INTERNATIONAL LLC] 3 Legacy NDC, 1 package rows 20211210_c396cf1b-b06a-4c29-b900-ee2db0905415.zip
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 60986-2030-5 60986203005 20 mL in 1 BOTTLE (60986-2030-5) 20 ml 2015-01-27 0000-00-00 No No Current