D-27

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 02:31:19

Label at a glance#

ProductD-27

Active ingredientBERBERIS VULGARIS ROOT BARK, NITRIC ACID, CALCIUM FLUORIDE, LYCOPODIUM CLAVATUM SPORE, RUBIA TINCTORUM ROOT, SMILAX ORNATA ROOT

Label structure8 sections

Storage and handling

SHAKE WELL

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

NDC 58264-0027-1

INDICATIONS

INDICATIONS & USAGE SECTION

OTC - PURPOSE SECTION

Sharp pains across the small of the back.

INGREDIENTS

OTC - ACTIVE INGREDIENT SECTION

ACTIVE

SPL UNCLASSIFIED SECTION

Berberis vulgaris 3x, Acidum nitricum 6x, Calcarea fluorica 12x, Lycopodium clavatum 5x, Rubia tinctorum 2x, Sarsaparilla 3x

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.

D 27

HOMEOPATHIC
STRESS FORMULA

1 FL. OZ.

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
58264-0027-1	2022-06-02	C162847	48780-1	9d75b9d0-50ce-f424-e053-dadaa90a57ce	D-27
58264-0027-1	2020-01-31	C162847	48780-1	9d75b9d0-50ce-f424-e053-dadaa90a57ce	D-27

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
58264-0027-1	D-27	29.57 mL in 1 BOTTLE, GLASS	SOLUTION/ DROPS	29.57		3

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
58264-0027	D-27 (BERBERIS VULGARIS ROOT BARK, NITRIC ACID, CALCIUM FLUORIDE, LYCOPODIUM CLAVATUM SPORE, RUBIA TINCTORUM ROOT, AND SMILAX ORNATA ROOT) SOLUTION/ DROPS [DNA LABS, INC.]	3	Current NDC, Legacy NDC, 1 package rows	20250115_85b13ca5-a35f-4118-93ce-985d4ea9258c.zip

Products#

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

DailyMed product names page 1 of 1 · 11 matching rows.

D-27
BERBERIS VULGARIS ROOT BARK, NITRIC ACID, CALCIUM FLUORIDE, LYCOPODIUM CLAVATUM SPORE, RUBIA TINCTORUM ROOT, and SMILAX ORNATA ROOT
ALCOHOL
WATER
BERBERIS VULGARIS ROOT BARK
NITRIC ACID
CALCIUM FLUORIDE
FLUORIDE ION
LYCOPODIUM CLAVATUM SPORE
RUBIA TINCTORUM ROOT
SMILAX ORNATA ROOT

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
58264-0027	58264-0027-1

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
Name	UNII	Kind
ALCOHOL	3K9958V90M	IACT
WATER	059QF0KO0R	IACT
BERBERIS VULGARIS ROOT BARK	1TH8Q20J0U	ACTIB
NITRIC ACID	411VRN1TV4	ACTIB
CALCIUM FLUORIDE	O3B55K4YKI	ACTIB
LYCOPODIUM CLAVATUM SPORE	C88X29Y479	ACTIB
RUBIA TINCTORUM ROOT	0SVP95L23G	ACTIB
SMILAX ORNATA ROOT	2H1576D5WG	ACTIB

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
D-27	BERBERIS VULGARIS ROOT BARK, NITRIC ACID, CALCIUM FLUORIDE, LYCOPODIUM CLAVATUM SPORE, RUBIA TINCTORUM ROOT, AND SMILAX ORNATA ROOT	DNA Labs, Inc.	85b13ca5-a35f-4118-93ce-985d4ea9258c	2025-01-13	Warnings	Exact identifier ndc (package): 58264-0027-1 ndc (product): 58264-0027 ndc11 (package): 58264002701 spl id: 2b9eb825-2e80-846c-e063-6394a90a0a7b spl set id: 85b13ca5-a35f-4118-93ce-985d4ea9258c

Reported adverse events (FAERS/openFDA)#

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