AB

Manufacturer: MARCO PHARMA INTERNATIONAL LLC | NESTMANN PHARMA
Effective date: 2026-01-12
Label type: HUMAN OTC DRUG LABEL
Version: 2
Source: full-release
Hydrated at: 2026-06-01 02:36:42

Label at a glance#

ProductAB

Active ingredientACONITUM NAPELLUS, BRYONIA CRETICA SUBSP. DIOICA ROOT

Label structure9 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

ACONITUM NAPELLUS 3X HPUS

BRYONIA CRETICA 3X HPUS

INACTIVE INGREDIENT SECTION

ETHYL ALCOHOL 20% V/V

WATER

OTC - PURPOSE SECTION

FOR TEMPORARY RELIEF OF MINOR INFLAMMATION AND TRAUMA

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF CHILDREN

OTC - PREGNANCY OR BREAST FEEDING SECTION

IF PREGNANT OR BREAST-FEEDING, CONSULT A HEALTH PROFESSIONAL BEFORE USE

WARNINGS SECTION

IF SYMPTOMS PERSIST MORE THAN A FEW DAYS, CONTACT LICENSED PRACTIONER.

INDICATIONS & USAGE SECTION

FOR TEMPORARY RELIEF OF MINOR INFLAMMATION AND TRAUMA

DOSAGE & ADMINISTRATION SECTION

DAY 1; TAKE 5 DROPS ON THE TONGUE EVERY 15 MINUTES FOR 2 HOURS. THEN TAKE 5 DROPS ONCE EVERY HOUR. DAY 2; TAKE 5 DROPS ONCE EVERY HOUR. DAY 3; TAKE 5 DROPS EVERY TWO HOURS. CONTINUE WITH 10 DROPS THREE TIMES DAILY

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

N11_60986-2040

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
60986-2040-3	AB	50 mL in 1 BOTTLE	LIQUID	50		2

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 6 matching rows.

AB
ACONITUM NAPELLUS, BRYONIA CRETICA
WATER
ALCOHOL
ACONITUM NAPELLUS
BRYONIA CRETICA SUBSP. DIOICA ROOT

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
60986-2040	60986-2040-3

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
WATER	059QF0KO0R	IACT
ALCOHOL	3K9958V90M	IACT
ACONITUM NAPELLUS	U0NQ8555JD	ACTIB
BRYONIA CRETICA SUBSP. DIOICA ROOT	53UB5FH7CX	ACTIB

Source Document#

Source XML

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
AB	ACONITUM NAPELLUS, BRYONIA CRETICA	MARCO PHARMA INTERNATIONAL LLC	2d81c13f-102a-6741-e063-6294a90aee84	2026-01-12	Warnings	Exact identifier ndc (package): 60986-2040-3 ndc (product): 60986-2040 ndc11 (package): 60986204003 spl id: 483ad8b7-56c6-1dc3-e063-6394a90abb23 spl set id: 2d81c13f-102a-6741-e063-6294a90aee84

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.