N-22

Manufacturer
DNA Labs, Inc.
Effective date
2022-12-29
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 02:19:10

Label at a glance#

ProductN-22
Active ingredientMERCURIUS SOLUBILIS, BARIUM CARBONATE, ATROPA BELLADONNA, POTASSIUM DICHROMATE, PHYTOLACCA AMERICANA WHOLE, ANEMONE PULSATILLA, BOS TAURUS PAROTID GLAND, APIS MELLIFERA, PILOCARPUS MICROPHYLLUS LEAF, FERROSOFERRIC PHOSPHATE, TRIFOLIUM REPENS WHOLE
Label structure8 sections

Storage and handling

SHAKE WELL

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

NDC 58264-0230-1

INDICATIONS & USAGE SECTION

OTC - PURPOSE SECTION

Support for the Parotid; Proper saliva production

OTC - ACTIVE INGREDIENT SECTION

SPL UNCLASSIFIED SECTION

Parotid 6/12/30/60/200x, Mercurius solubilis 9x, Baryta carbonica, Ferrum phosphoricum, Kalium bichromicum, Phytolacca decandra, Pulsatilla 6x, Belladonna 5x, Apis mellifica, Jaborandi, Trifolium repens 4x

INACTIVE INGREDIENT SECTION

20% alcohol in purified water.

DOSAGE & ADMINISTRATION SECTION

One dropper under tongue two times daily. Acute symptoms 1/2 dropper under tongue every 30 minutes for two hours.

STORAGE AND HANDLING SECTION

SHAKE WELL

WARNINGS 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.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

DYNAMIC

NUTRITIONAL

ASSOCIATES, INC.

N-22

PAROTID ENERGIZER

HOMEOPATHIC ENDOCRINE

1 FL. OZ.

N-22N-22

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
58264-0230-12025-01-30C16284748780-12cef2736-812b-d83d-e063-dadaa90ab31fN-22

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
58264-0230-1N-2229.57 mL in 1 BOTTLE, GLASSSOLUTION29.571

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
58264-0230N-22 (APIS MELLIFERA, PILOCARPUS MICROPHYLLUS LEAF, TRIFOLIUM REPENS WHOLE, ATROPA BELLADONNA, BARIUM CARBONATE, FERROSOFERRIC PHOSPHATE, POTASSIUM DICHROMATE, PHYTOLACCA AMERICANA WHOLE, ANEMONE PULSATILLA, MERCURIUS SOLUBILIS AND BOS TAURUS PAROTID GLAND) SOLUTION [DNA LABS, INC.]1Legacy NDC, 1 package rows20230101_f0ffc043-bfe3-5986-e053-2995a90a7ec1.zip

Products#

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

DailyMed product names page 1 of 1 · 17 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
58264-023058264-0230-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 13 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
f0ffc043-bfe4-5986-e053-2995a90a7ec1f0ffc043-bfe3-5986-e053-2995a90a7ec12022-12-29WarningsExact identifier
spl id: f0ffc043-bfe4-5986-e053-2995a90a7ec1
spl set id: f0ffc043-bfe3-5986-e053-2995a90a7ec1

Reported adverse events (FAERS/openFDA)#

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