AM-2

Manufacturer: DNA Labs, Inc.
Effective date: 2025-01-09
Label type: HUMAN OTC DRUG LABEL
Version: 3
Source: full-release
Hydrated at: 2026-06-01 02:30:15

Label at a glance#

ProductAM-2

Active ingredientCOLCHICUM AUTUMNALE WHOLE, SODIUM SULFATE ANHYDROUS, NAJA NAJA WHOLE

Label structure8 sections

Storage and handling

SHAKE WELL

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

NDC 58264-0341-1

INDICATIONS

INDICATIONS & USAGE SECTION

OTC - PURPOSE SECTION

Regulates energy flow through the heart meridian.

INGREDIENTS

OTC - ACTIVE INGREDIENT SECTION

ACTIVE

SPL UNCLASSIFIED SECTION

Colchicum autumnale 12x, Natrum sulphuricum 8x, Naja tripudians 12x

INACTIVE

INACTIVE INGREDIENT SECTION

20% alcohol in purified water.

SUGGESTED DOSAGE

DOSAGE & ADMINISTRATION SECTION

5 to 10 drops twice a day, meridian energy excess 1 to 5 drops t.i.d, meridian lacking in energy 10 to 20 drops t.i.d.

STORAGE AND HANDLING SECTION

SHAKE WELL

Warnings

WARNINGS SECTION

SPL UNCLASSIFIED SECTION

Use only if cap seal is unbroken.

OTC - PREGNANCY OR BREAST FEEDING SECTION

If pregnant or breastfeeding, ask a healthcare professional before use.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep this and all medication out of the reach of children.

SPL UNCLASSIFIED SECTION

To be used according to standard homeopathic indications.

PRINCIPAL DISPLAY PANEL - 1 FL. OZ. Bottle Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

DYNAMIC
NUTRITIONAL
ASSOCIATES, INC.

AM-2
HEART

ACUPUNCTURE MERIDIAN

1 FL. OZ.

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
95250459-30e4-45c1-b08a-993044f49109	Product name	2	20250805
362d7abb-94e6-4c60-9a58-266894157713	Product name	1	20231023
9badc7be-250a-44ab-aa36-926af3f02679	Product name	1	20210527
816b97af-edc5-4060-aff1-b814bdbcad50	Product name	1	20190415
26acd337-b838-40ac-bcbc-05c3b81c8712	Product name	1	20170323

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
58264-0341-1	2022-06-02	C162847	48780-1	9d75b9cf-ce7e-f424-e053-dadaa90a57ce	AM-2
58264-0341-1	2020-01-31	C162847	48780-1	9d75b9cf-ce7e-f424-e053-dadaa90a57ce	AM-2

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
58264-0341-1	AM-2	29.57 mL in 1 BOTTLE, GLASS	SOLUTION	29.57		3

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
58264-0341	AM-2 (COLCHICUM AUTUMNALE WHOLE, SODIUM SULFATE ANHYDROUS, AND NAJA NAJA WHOLE) SOLUTION [DNA LABS, INC.]	3	Current NDC, Legacy NDC, 1 package rows	20250112_2839f10b-897b-41cb-b0ca-c2e051765d5c.zip

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

AM-2
COLCHICUM AUTUMNALE WHOLE, SODIUM SULFATE ANHYDROUS, and NAJA NAJA WHOLE
ALCOHOL
WATER
COLCHICUM AUTUMNALE WHOLE
SODIUM SULFATE ANHYDROUS
SULFATE ION
NAJA NAJA WHOLE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
58264-0341	58264-0341-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
ALCOHOL	3K9958V90M	IACT
WATER	059QF0KO0R	IACT
COLCHICUM AUTUMNALE WHOLE	W79255C628	ACTIB
SODIUM SULFATE ANHYDROUS	36KCS0R750	ACTIR
NAJA NAJA WHOLE	D279BDR31E	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
AM-2	COLCHICUM AUTUMNALE WHOLE, SODIUM SULFATE ANHYDROUS, AND NAJA NAJA WHOLE	DNA Labs, Inc.	2839f10b-897b-41cb-b0ca-c2e051765d5c	2025-01-09	Warnings	Exact identifier ndc (package): 58264-0341-1 ndc (product): 58264-0341 ndc11 (package): 58264034101 spl id: 2b52d8d8-5796-e0ae-e063-6394a90af1e6 spl set id: 2839f10b-897b-41cb-b0ca-c2e051765d5c

Reported adverse events (FAERS/openFDA)#

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