Other
NDC 58264-0003-1
- Use only if cap seal is unbroken.
To be used according to standard homeopathic indications.
D3
FDA Label NDC 58264-0003
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Dna Labs, Inc. for the product D3 (NDC 58264-0003). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding other, otc - purpose, ingredients, rx caution, suggested dosage, storage and handling, otc - pregnancy or breast feeding, otc - keep out of reach of children, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Otc - Purpose
Heart insufficiencies.
Ingredients
Digitalis purpurea 4x, Strophanthus 6x, Crataegus oxyacantha 1x, Cactus grandiflorus 2x, Kalmia latifolia 3x, Arsenicum album 5x, Phosphorus 5x, Scilla maritima 4x, Spigelia anthelmia 3x, Kalium carbonicum 4x, 20% alcohol in purified water.
Rx Caution
Federal law prohibits dispensing without a prescription.
Suggested Dosage
One dropper full under the tongue two times daily. In acute conditions 5-10 drops under the tongue every 20-30 minutes.
Storage And Handling
SHAKE WELL
Otc - Pregnancy Or Breast Feeding
- 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
- Keep this and all medication out of the reach of children.
Principal Display Panel - 1 Fl. Oz. Bottle Label
DYNAMIC
NUTRITIONAL
ASSOCIATES, INC.
D 3
HOMEOPATHIC FORMULA
1 FL. OZ.
Principal Display Panel (1 FL. OZ. Bottle Label)
* Please review the disclaimer below.
