FDA.reportPublic FDA data

D-46

Manufacturer
DNA Labs, Inc.
Effective date
2025-01-13
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
full-release
Hydrated at
2026-06-01 02:31:23

Label at a glance#

ProductD-46
Active ingredientFERROSOFERRIC PHOSPHATE, LITHIUM CARBONATE, SODIUM SULFATE, STRYCHNOS NUX-VOMICA SEED, RHODODENDRON AUREUM LEAF, FILIPENDULA ULMARIA ROOT
Label structure9 sections

Storage and handling

SHAKE WELL

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

NDC 58264-0046-1

INDICATIONS

INDICATIONS & USAGE SECTION

OTC - PURPOSE SECTION

Rheumatism, gout, swollen joints.

INGREDIENTS

OTC - ACTIVE INGREDIENT SECTION

ACTIVE

SPL UNCLASSIFIED SECTION

Ferrum phosphoricum 12x, Lithium carbonicum 12x, Natrum sulfuricum 30x, Nux vomica 30x, Rhododendron chrysanthum 6x, Spiraea ulmaria 12x

INACTIVE

INACTIVE INGREDIENT SECTION

20% alcohol in purified water.

Rx CAUTION

SPL UNCLASSIFIED SECTION

Federal law prohibits dispensing without a prescription.

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 46

HOMEOPATHIC


STRESS FORMULA

1 FL. OZ.

D-46D-46

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
95250459-30e4-45c1-b08a-993044f49109Product name220250805
b3053bb1-353b-4a0b-bca5-28fe7228957cProduct name220250124
362d7abb-94e6-4c60-9a58-266894157713Product name120231023
9badc7be-250a-44ab-aa36-926af3f02679Product name120210527
816b97af-edc5-4060-aff1-b814bdbcad50Product name120190415
8ce6e144-236f-b7be-f690-f06e0c8c6bd3Product name220170725
26acd337-b838-40ac-bcbc-05c3b81c8712Product name120170323
f09af6ee-c6dd-d0ce-77ad-93508bcdacedProduct name420161205

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
58264-0046-12022-06-02C16284748780-19d75b9d1-027c-f424-e053-dadaa90a57ceD-46
58264-0046-12020-01-31C16284748780-19d75b9d1-027c-f424-e053-dadaa90a57ceD-46

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
58264-0046-1D-4629.57 mL in 1 BOTTLE, GLASSSOLUTION29.575

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
58264-0046D-46 (FERROSOFERRIC PHOSPHATE, LITHIUM CARBONATE, SODIUM SULFATE, STRYCHNOS NUX-VOMICA SEED, RHODODENDRON AUREUM LEAF, AND FILIPENDULA ULMARIA ROOT) SOLUTION [DNA LABS, INC.]5Current NDC, Legacy NDC, 1 package rows20250115_be8b4acb-83c6-4d25-ba90-ee6e6e0a588e.zip

Products#

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

DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
58264-004658264-0046-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALCOHOL3K9958V90MIACT
WATER059QF0KO0RIACT
FERROSOFERRIC PHOSPHATE91GQH8I5F7ACTIB
LITHIUM CARBONATE2BMD2GNA4VACTIB
SODIUM SULFATE0YPR65R21JACTIB
STRYCHNOS NUX-VOMICA SEED269XH13919ACTIB
RHODODENDRON AUREUM LEAFIV92NQJ73UACTIB
FILIPENDULA ULMARIA ROOT997724QNDSACTIB

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-46FERROSOFERRIC PHOSPHATE, LITHIUM CARBONATE, SODIUM SULFATE, STRYCHNOS NUX-VOMICA SEED, RHODODENDRON AUREUM LEAF, AND FILIPENDULA ULMARIA ROOTDNA Labs, Inc.be8b4acb-83c6-4d25-ba90-ee6e6e0a588e2025-01-13WarningsExact identifier
ndc (package): 58264-0046-1
ndc (product): 58264-0046
ndc11 (package): 58264004601
spl id: 2b9eb825-2e82-846c-e063-6394a90a0a7b
spl set id: be8b4acb-83c6-4d25-ba90-ee6e6e0a588e

Reported adverse events (FAERS/openFDA)#

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