FDA.reportPublic FDA data

D1

Manufacturer
DNA Labs, Inc.
Effective date
2018-01-29
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 02:09:12

Label at a glance#

ProductD1
Active ingredientAPIS MELLIFERA, BELLADONNA LEAF, MERCURIC CHLORIDE, BARIUM CHLORIDE DIHYDRATE, LACHESIS MUTA VENOM, CALCIUM IODIDE, CALCIUM SULFIDE, POTASSIUM DICHROMATE, TEUCRIUM MARUM, PHYTOLACCA AMERICANA WHOLE
Label structure8 sections

Storage and handling

SHAKE WELL

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

NDC 58264-0001-1

INDICATIONS & USAGE SECTION

INDICATIONS

OTC - PURPOSE SECTION

Acute and chronic inflammation.

OTC - ACTIVE INGREDIENT SECTION

INGREDIENTS

INACTIVE INGREDIENT SECTION

Apis mellifica 4x, Belladonna 4x, Mercurius corrosivus 6x, Baryta muriatica 6x, Lachesis mutus 12x, Calcarea iodata 6x, Hepar sulfuris calcareum 12x, Kalium bichromicum 4x, Teucrium marum verum 6x, Phytolacca decandra 4x, 20% alcohol in purified water.

SUGGESTED DOSAGE

DOSAGE & ADMINISTRATION SECTION

One dropper full under the tongue two times daily. In acute conditions 5-10 drops under the tongue every 20-30 minutes.

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.

D 1

HOMEOPATHIC FORMULA

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
bee4fa8d-8d82-423a-a0b5-40a89dd13a99Product name120250618
e0d2eb29-08bd-4bba-90d1-c91c68a38767Product name420250516
30b0ac6e-02aa-0e5c-0d8b-cffdf3a282b2Product name520250304
334fe8d2-68fb-4331-a576-420e302ec069Product name720240320
444b3e50-f226-46ef-bfca-2e7035d140cdProduct name120190611
e92765c1-be81-432a-b909-1b10777ec378Product name120190208
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
d5e51f11-ad28-caa4-4b49-4143974782adProduct name120150831
0ca1d589-929b-4b33-bc5b-1d84abdafa6aProduct name120150324
fc363c46-397b-4476-ac0f-70e43e8e4592Product name120150324
0441a8f5-3835-497c-aedd-bc78cba56b2aProduct name120150317
87711080-88eb-65c5-b2dd-bf99e700a372Product name120140508
ec2149b3-5c6d-5344-f757-c86411073075Product name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
58264-0001-12020-01-31C16284748780-19d75b9d0-94e1-f424-e053-dadaa90a57ceD1

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
58264-0001-1D129.57 mL in 1 BOTTLE, GLASSSOLUTION29.571

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
58264-0001D1 (APIS MELLIFERA, BELLADONNA LEAF, MERCURIC CHLORIDE, BARIUM CHLORIDE DIHYDRATE, LACHESIS MUTA VENOM, CALCIUM IODIDE, CALCIUM SULFIDE, POTASSIUM DICHROMATE, TEUCRIUM MARUM, AND PHYTOLACCA AMERICANA WHOLE) SOLUTION [DNA LABS, INC.]1Legacy NDC, 1 package rows20180131_e27ff5aa-598a-4464-b3ce-9ae8e6bf95b1.zip

Products#

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

DailyMed product names page 1 of 1 · 18 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
58264-000158264-0001-1

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
APIS MELLIFERA7S82P3R43ZACTIB
BELLADONNA LEAF6GZW20TIOIACTIB
MERCURIC CHLORIDE53GH7MZT1RACTIB
BARIUM CHLORIDE DIHYDRATEEL5GJ3U77EACTIB
LACHESIS MUTA VENOMVSW71SS07IACTIB
CALCIUM IODIDE8EKI9QEE2HACTIB
CALCIUM SULFIDE1MBW07J51QACTIB
POTASSIUM DICHROMATET4423S18FMACTIB
TEUCRIUM MARUM10464S0TAAACTIB
PHYTOLACCA AMERICANA WHOLE9SM28U1ELRACTIB
Alcohol3K9958V90MIACT
Water059QF0KO0RIACT

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
310368cf-c4eb-4b12-bff1-6e683bd08bebe27ff5aa-598a-4464-b3ce-9ae8e6bf95b12018-01-29WarningsExact identifier
spl id: 310368cf-c4eb-4b12-bff1-6e683bd08beb
spl set id: e27ff5aa-598a-4464-b3ce-9ae8e6bf95b1

Reported adverse events (FAERS/openFDA)#

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