Other
NDC 58264-0002-1
- Use only if cap seal is unbroken.
To be used according to standard homeopathic indications.
D2
FDA Label NDC 58264-0002
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 D2 (NDC 58264-0002). 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, indications, 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
Indications
Organic and functional affections of the heart.
Ingredients
Aurum muriaticum 6x, Crataegus oxyacantha 1x, Cactus grandiflorus 4x, Kalium phosphoricum 4x, Aconitum napellus 6x, Valeriana officinalis 3x, Spigelia anthelmia 4x, Arnica montana 4x, Digitalis purpurea 4x, Laurocerasus 4x, Ignatia amara 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.
D2
HOMEOPATHIC FORMULA
1 FL. OZ.
Principal Display Panel (1 FL. OZ. Bottle Label)
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