T-29

Manufacturer
DNA Labs, Inc.
Effective date
2025-01-09
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
full-release
Hydrated at
2026-06-01 02:31:03

Label at a glance#

ProductT-29
Active ingredientORNITHOGALUM UMBELLATUM
Label structure7 sections

Storage and handling

SHAKE WELL

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

NDC 58264-0274-1

INDICATIONS & USAGE SECTION

INDICATIONS

OTC - PURPOSE SECTION

After effect of shock, mental or physical.

OTC - ACTIVE INGREDIENT SECTION

INGREDIENTS

INACTIVE INGREDIENT SECTION

Ornithogalum umbellatum 6/8/30x, 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

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.

T-29

STAR OF BETHLEHEM

FLOWER ESSENCES

1 FL. OZ.

T-29 DIST Label Proof 4.22.jpgT-29 DIST Label Proof 4.22.jpg

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
58264-0274-12020-01-31C16284748780-19d75b9d0-69ee-f424-e053-dadaa90a57ceT-29

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
58264-0274-1T-2929.57 mL in 1 BOTTLE, GLASSSOLUTION29.575

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
58264-0274T-29 (ORNITHOGALUM UMBELLATUM) SOLUTION [DNA LABS, INC.]5Current NDC, Legacy NDC, 1 package rows20250112_d21e6bb7-810e-4da4-9361-00c7805998a8.zip

Products#

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

DailyMed product names page 1 of 1 · 4 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
58264-027458264-0274-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALCOHOL3K9958V90MIACT
WATER059QF0KO0RIACT
ORNITHOGALUM UMBELLATUM9NS3M2Y78SACTIB

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
T-29ORNITHOGALUM UMBELLATUMDNA Labs, Inc.d21e6bb7-810e-4da4-9361-00c7805998a82025-01-09WarningsExact identifier
ndc (package): 58264-0274-1
ndc (product): 58264-0274
ndc11 (package): 58264027401
spl id: 2b53b6a7-5806-18fb-e063-6294a90a270c
spl set id: d21e6bb7-810e-4da4-9361-00c7805998a8

Reported adverse events (FAERS/openFDA)#

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