N-12 NDC 58264-0210

NDC codes

FDA NDC Directory

Product NDC (as listed)58264-0210Labeler and product segments. Claims need a package NDC.

Product NDC at billing width58264-0210Add the package segment from the table below.

Package NDCs as listed with the FDA, and the 11-digit 5-4-2 form used on claims. The highlighted digit is the added leading zero.
Package NDC	11-digit (billing)	Package	Copy
58264-0210-1	58264021001	29.57 mL in 1 BOTTLE, GLASS (58264-0210-1)Marketed from Jan 1, 1990

How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules

Product information

Brand name (proprietary): N-12
Generic name (nonproprietary): phosphoric acid, cinchona officinalis bark, anemone pulsatilla, phosphorus, picric acid, magnesium phosphate, dibasic trihydrate, viburnum opulus whole, bos taurus pituitary gland, posterior, bos taurus ovary, bos taurus adrenal gland, and thyroid, unspecified
Active ingredients: Phosphoric acid — 6 [hp_X]/mLCinchona officinalis bark — 6 [hp_X]/mLAnemone pulsatilla — 6 [hp_X]/mLPhosphorus — 6 [hp_X]/mLPicric acid — 6 [hp_X]/mLMagnesium phosphate, Dibasic trihydrate — 6 [hp_X]/mLViburnum opulus whole — 2 [hp_X]/mLBos taurus pituitary gland, Posterior — 200 [hp_X]/mLBos taurus ovary — 200 [hp_X]/mLBos taurus adrenal gland — 200 [hp_X]/mLThyroid, Unspecified — 200 [hp_X]/mL
Dosage form: Solution
Route: Sublingual
Labeler: DNA Labs, Inc.
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Jan 1, 1990
Listing expires: Dec 31, 2026
Other FDA classes: Increased Large Intestinal Motility (Physiologic effect)Inhibition Large Intestine Fluid/Electrolyte Absorption (Physiologic effect)Inhibition Small Intestine Fluid/Electrolyte Absorption (Physiologic effect)Magnesium Ion Exchange Activity (Mechanism)Osmotic Activity (Mechanism)Stimulation Large Intestine Fluid/Electrolyte Secretion (Physiologic effect)
Identifiers: Product ID 58264-0210_2b539b74-75a3-e36c-e063-6294a90ae2ddSPL ID 2b539b74-75a3-e36c-e063-6294a90ae2ddSPL set ID 89ed00b4-5739-439e-bae9-e00b0b0d7222UNII E4GA8884NN, S003A158SB, I76KB35JEV, 27YLU75U4W, A49OS0F91S, HF539G9L3Q, DIO510WJ04, 7JM57I419K, 66LZN1C747, M2776SWB29, 0B4FDL9I6P
Pharmacologic class: Calculi Dissolution Agent; Osmotic Laxative

Billing references

What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.

HCPCS codeNo match

No HCPCS code in Med-Code's directory. Sublingual products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N458264021001 followed by a unit qualifier and the quantity

Package 58264-0210-01. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier

Product label

Current FDA label (SPL), effective Jan 9, 2025.

Indications (excerpt from the label)

INDICATIONS Physical weakness, mood swings, and premenstrual difficulties in women.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)