FDA.reportPublic FDA data

D-26

Manufacturer
DNA Labs, Inc.
Effective date
2025-01-13
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 02:31:16

Label at a glance#

ProductD-26
Active ingredientFERROUS IODIDE, PHOSPHORIC ACID, SULFUR IODIDE, CALCIUM IODIDE, NITRIC ACID
Label structure8 sections

Storage and handling

SHAKE WELL

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

NDC 58264-0026-1

INDICATIONS

INDICATIONS & USAGE SECTION

OTC - PURPOSE SECTION

Draining and stimulating immune system

INGREDIENTS

OTC - ACTIVE INGREDIENT SECTION

ACTIVE

SPL UNCLASSIFIED SECTION

Ferrum iodatum 12x, Acidum phosphoricum 12x, Sulphur iodatum 12x, Calcarea iodata 12x, Acidum nitricum 12x

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.

D 26

HOMEOPATHIC
STRESS 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
58264-0026-12022-06-02C16284748780-19d75b9d0-2467-f424-e053-dadaa90a57ceD-26
58264-0026-12020-01-31C16284748780-19d75b9d0-2467-f424-e053-dadaa90a57ceD-26

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
58264-0026-1D-2629.57 mL in 1 BOTTLE, GLASSSOLUTION/ DROPS29.573

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
58264-0026D-26 (FERROUS IODIDE, PHOSPHORIC ACID, SULFUR IODIDE, CALCIUM IODIDE, AND NITRIC ACID) SOLUTION/ DROPS [DNA LABS, INC.]3Current NDC, Legacy NDC, 1 package rows20250115_5ef26695-7b71-4c01-a60c-f72dd1fa342d.zip

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
58264-002658264-0026-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALCOHOL3K9958V90MIACT
WATER059QF0KO0RIACT
FERROUS IODIDEF5452U54PNACTIB
PHOSPHORIC ACIDE4GA8884NNACTIB
SULFUR IODIDEL6L8KA2AA0ACTIB
CALCIUM IODIDE8EKI9QEE2HACTIB
NITRIC ACID411VRN1TV4ACTIB

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
D-26FERROUS IODIDE, PHOSPHORIC ACID, SULFUR IODIDE, CALCIUM IODIDE, AND NITRIC ACIDDNA Labs, Inc.5ef26695-7b71-4c01-a60c-f72dd1fa342d2025-01-13WarningsExact identifier
ndc (package): 58264-0026-1
ndc (product): 58264-0026
ndc11 (package): 58264002601
spl id: 2b9ea85a-20ed-8fa9-e063-6294a90a9ef1
spl set id: 5ef26695-7b71-4c01-a60c-f72dd1fa342d

Reported adverse events (FAERS/openFDA)#

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