FDA.reportPublic FDA data

N-22

Manufacturer
DNA Labs, Inc.
Effective date
2022-06-06
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 22:00:06

Label at a glance#

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

Storage and handling

SHAKE WELL

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

NDC 58264-0220-1

INDICATIONS

INDICATIONS & USAGE SECTION

OTC - PURPOSE SECTION

Support for the Parotid; Proper saliva production.

INGREDIENTS

OTC - ACTIVE INGREDIENT SECTION

ACTIVE

SPL UNCLASSIFIED SECTION

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

INACTIVE

INACTIVE INGREDIENT SECTION

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

  • 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.

N-22
PAROTID ENERGIZER

HOMEOPATHIC ENDOCRINE

1 FL. OZ.

Principal Display Panel - 1 FL. OZ. Bottle Label
Principal Display Panel - 1 FL. OZ. Bottle Label

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
58264-0220-12022-06-06C16284748780-19d75b9d0-962e-f424-e053-dadaa90a57ceN-22
58264-0220-12020-01-31C16284748780-19d75b9d0-962e-f424-e053-dadaa90a57ceN-22

Products#

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

DailyMed product names page 1 of 1 · 16 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
58264-022058264-0220-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 12 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALCOHOL3K9958V90MIACT
WATER059QF0KO0RIACT
APIS MELLIFERA7S82P3R43ZACTIB
PILOCARPUS MICROPHYLLUS LEAFTY68V0X4KLACTIB
TRIFOLIUM REPENS WHOLEM28256480LACTIB
ATROPA BELLADONNAWQZ3G9PF0HACTIB
BARIUM CARBONATE6P669D8HQ8ACTIB
FERROSOFERRIC PHOSPHATE91GQH8I5F7ACTIB
POTASSIUM DICHROMATET4423S18FMACTIB
PHYTOLACCA AMERICANA WHOLE9SM28U1ELRACTIB
ANEMONE PULSATILLAI76KB35JEVACTIB
BOS TAURUS PAROTID GLAND6NWC5E4H38ACTIB

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
2b539b74-75a7-e36c-e063-6294a90ae2ddd5ee45a0-c9cb-4ba3-99b0-0a6d85a79ab12025-01-09WarningsExact identifier
spl set id: d5ee45a0-c9cb-4ba3-99b0-0a6d85a79ab1

Reported adverse events (FAERS/openFDA)#

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