T-24

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 02:31:07

Label at a glance#

ProductT-24
Active ingredientPINUS SYLVESTRIS WHOLE
Label structure8 sections

Storage and handling

SHAKE WELL

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

NDC 58264-0269-1

INDICATIONS

INDICATIONS & USAGE SECTION

OTC - PURPOSE SECTION

Self-reproach, guilt feelings, despondency.

INGREDIENTS

OTC - ACTIVE INGREDIENT SECTION

ACTIVE

SPL UNCLASSIFIED SECTION

Pinus sylvestris 6/8/30x

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

SPL UNCLASSIFIED 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.

T-24

PINE

FLOWER ESSENCES

1 FL. OZ.

T-24 DIST Label Proof 4.22.jpgT-24 DIST Label Proof 4.22.jpg

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
58264-0269-12020-01-31C16284748780-19d75b9cf-cdeb-f424-e053-dadaa90a57ceT-24

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
58264-0269-1T-2429.57 mL in 1 BOTTLE, GLASSSOLUTION29.575

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
58264-0269T-24 (PINUS SYLVESTRIS WHOLE) SOLUTION [DNA LABS, INC.]5Current NDC, Legacy NDC, 1 package rows20250112_fe4066cd-89bc-4c86-bd97-aa3a2f1f2a9e.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
58264-026958264-0269-1

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
PINUS SYLVESTRIS WHOLEVP00HZL9ICACTIB

Source Document#

Source XML · Source PDF

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-24PINUS SYLVESTRIS WHOLEDNA Labs, Inc.fe4066cd-89bc-4c86-bd97-aa3a2f1f2a9e2025-01-09WarningsExact identifier
ndc (package): 58264-0269-1
ndc (product): 58264-0269
ndc11 (package): 58264026901
spl id: 2b53b6a7-5805-18fb-e063-6294a90a270c
spl set id: fe4066cd-89bc-4c86-bd97-aa3a2f1f2a9e

Reported adverse events (FAERS/openFDA)#

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