Drugplain

N-21 8 [hp_X]/mL

calcium fluoride, silicon dioxide, euphrasia stricta, ruta graveolens whole, gelsemium sempervirens whole, physostigma venenosum whole, anemone pulsatilla, sodium chloride, and sus scrofa eye · SOLUTION · DNA Labs, Inc.

No Recall HistoryCurrently in Shortage
Plain English

N-21 is a solution containing calcium fluoride, silicon dioxide, euphrasia stricta, ruta graveolens whole, gelsemium sempervirens whole, physostigma venenosum whole, anemone pulsatilla, sodium chloride, and sus scrofa eye at 8 [hp_X]/mL, taken sublingual. Manufactured by DNA Labs, Inc..

Key Facts

Brand Name
N-21
Generic Name
calcium fluoride, silicon dioxide, euphrasia stricta, ruta graveolens whole, gelsemium sempervirens whole, physostigma venenosum whole, anemone pulsatilla, sodium chloride, and sus scrofa eye
NDC Code (Product)
58264-0219
Manufacturer
DNA Labs, Inc.
Strength
8 [hp_X]/mL
Dosage Form
SOLUTION
Route
SUBLINGUAL
Marketing Status
Marketing Start
01/01/1990

Recall History

No Recall History

Frequently Asked Questions

What is N-21 used for?

N-21 contains calcium fluoride, silicon dioxide, euphrasia stricta, ruta graveolens whole, gelsemium sempervirens whole, physostigma venenosum whole, anemone pulsatilla, sodium chloride, and sus scrofa eye. It is a solution taken sublingual. Consult your doctor for specific uses.

Is N-21 a controlled substance?

N-21 is not classified as a controlled substance by the DEA.

What is the generic name for N-21?

The generic name for N-21 is calcium fluoride, silicon dioxide, euphrasia stricta, ruta graveolens whole, gelsemium sempervirens whole, physostigma venenosum whole, anemone pulsatilla, sodium chloride, and sus scrofa eye. There are no other listed brand versions of calcium fluoride, silicon dioxide, euphrasia stricta, ruta graveolens whole, gelsemium sempervirens whole, physostigma venenosum whole, anemone pulsatilla, sodium chloride, and sus scrofa eye.

What is the NDC code for N-21 8 [hp_X]/mL?

The NDC (National Drug Code) for N-21 8 [hp_X]/mL is 58264-0219, listed by DNA Labs, Inc..

Product NDC

58264-0219

Package NDC

58264-0219-1

Not medical advice. Always consult your doctor or pharmacist before making any medication decisions.

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