N-20

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 02:30:12

Label at a glance#

ProductN-20
Active ingredientSTRYCHNOS NUX-VOMICA SEED, ARSENIC TRIOXIDE, ACTIVATED CHARCOAL, SILVER NITRATE, MARSDENIA CUNDURANGO WHOLE, TRIPE, SUS SCROFA DUODENUM
Label structure8 sections

Storage and handling

SHAKE WELL

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

NDC 58264-0218-1

INDICATIONS

INDICATIONS & USAGE SECTION

OTC - PURPOSE SECTION

Support for the stomach; peptic ulcers; flatulence.

INGREDIENTS

OTC - ACTIVE INGREDIENT SECTION

INACTIVE INGREDIENT SECTION

Nux vomica 4x, Arsenicum album 6x, Carbo vegetabilis 10x, Argentum nitricum 6x, Condurango 6x, Stomach 6/12/30/60/200x, Duodenum 6/12/30/60/200x, 20% alcohol in purified water.

SUGGESTED DOSAGE

DOSAGE & ADMINISTRATION SECTION

One dropper under tongue two times daily. Acute symptoms ½ dropper under tongue every 30 minutes for two hours.

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

  • As with drugs if you are pregnant or nursing a baby seek professional advice before using this product.

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.

N-20
STOMACH ENERGIZER

HOMEOPATHIC ENDOCRINE

1 FL. OZ.

PRINCIPAL DISPLAY PANEL - 1 FL. OZ. Bottle Label
PRINCIPAL DISPLAY PANEL - 1 FL. OZ. Bottle Label

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
63f39a63-5cd1-4016-bd86-2bbb0f6c3139Product name320240506
e5a77e9c-c528-733a-173d-914a234c024bProduct name520240506
7792dadb-52b6-46b6-8fdf-80b1171065b5Product name120180810
6cca4355-1206-91f7-02de-17eef38a8622Product name120140508
751c581a-bf64-2fd7-b3ec-ca02c83e4a00Product name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
58264-0218-12022-06-06C16284748780-19d75b9d0-b66b-f424-e053-dadaa90a57ceN-20
58264-0218-12020-01-31C16284748780-19d75b9d0-b66b-f424-e053-dadaa90a57ceN-20

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
58264-0218-1N-2029.57 mL in 1 BOTTLE, GLASSSOLUTION29.573

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
58264-0218N-20 (STRYCHNOS NUX-VOMICA SEED, ARSENIC TRIOXIDE, ACTIVATED CHARCOAL, SILVER NITRATE, MARSDENIA CUNDURANGO WHOLE, TRIPE, AND SUS SCROFA DUODENUM) SOLUTION [DNA LABS, INC.]3Current NDC, Legacy NDC, 1 package rows20250112_14304769-22a0-4c0c-a79c-e70e1bc75cb6.zip

Products#

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

DailyMed product names page 1 of 1 · 13 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
58264-021858264-0218-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

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
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
N-20STRYCHNOS NUX-VOMICA SEED, ARSENIC TRIOXIDE, ACTIVATED CHARCOAL, SILVER NITRATE, MARSDENIA CUNDURANGO WHOLE, TRIPE, AND SUS SCROFA DUODENUMDNA Labs, Inc.14304769-22a0-4c0c-a79c-e70e1bc75cb62025-01-09WarningsExact identifier
ndc (package): 58264-0218-1
ndc (product): 58264-0218
ndc11 (package): 58264021801
spl id: 2b53985a-2338-fd8d-e063-6294a90a8bbc
spl set id: 14304769-22a0-4c0c-a79c-e70e1bc75cb6

Reported adverse events (FAERS/openFDA)#

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