D-111

Manufacturer
DNA Labs, Inc.
Effective date
2025-01-13
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 20:42:42

Label at a glance#

ProductD-111
Active ingredientMATRICARIA CHAMOMILLA, RHEUM OFFICINALE ROOT, ATROPA BELLADONNA, ARABICA COFFEE BEAN, TRIBASIC CALCIUM PHOSPHATE, CALCIUM FLUORIDE, MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE, OYSTER SHELL CALCIUM CARBONATE, CRUDE, WOOD CREOSOTE
Label structure8 sections

Storage and handling

SHAKE WELL

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

NDC 58264-0117-1

INDICATIONS

INDICATIONS & USAGE SECTION

OTC - PURPOSE SECTION

Teething children, tendency to cry, pain and sore gums.

INGREDIENTS

OTC - ACTIVE INGREDIENT SECTION

ACTIVE

SPL UNCLASSIFIED SECTION

Chamomilla vulgaris 30x, Rheum officinale 4x, 12x, Belladonna 4x, 30x, Coffea Cruda 6x, 30x, Calcarea phosphoricum 6x, 30x, Calcarea fluorica 8x, 30x, Magnesia phosphoricum 4x, 12x, Calcarea carbonica 8x, 30x, Kreosotum 6x, 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

  • 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 111

HOMEOPATHIC
STRESS FORMULA

1 FL. OZ.

PRINCIPAL DISPLAY PANEL - 1 FL. OZ. Bottle Label
PRINCIPAL DISPLAY PANEL - 1 FL. OZ. Bottle Label

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
58264-0117-12022-06-06C16284748780-19d75b9d0-3649-f424-e053-dadaa90a57ceD-111
58264-0117-12020-01-31C16284748780-19d75b9d0-3649-f424-e053-dadaa90a57ceD-111

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
58264-0117D-111 (MATRICARIA CHAMOMILLA, RHEUM OFFICINALE ROOT, ATROPA BELLADONNA, ARABICA COFFEE BEAN, TRIBASIC CALCIUM PHOSPHATE, CALCIUM FLUORIDE, MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE, OYSTER SHELL CALCIUM CARBONATE, CRUDE, AND WOOD CREOSOTE) SOLUTION [DNA LABS, INC.]3Legacy NDC20250115_5183ad26-c8cf-4c78-9d95-82ea4d696215.zip

Products#

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

DailyMed product names page 1 of 1 · 16 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
58264-011758264-0117-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 11 matching rows.

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
4bd38707-fb4b-58c2-e063-6394a90a3c515183ad26-c8cf-4c78-9d95-82ea4d6962152026-02-27WarningsExact identifier
spl set id: 5183ad26-c8cf-4c78-9d95-82ea4d696215

Reported adverse events (FAERS/openFDA)#

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