D14 NDC 58264-1014

NDC codes

FDA NDC Directory

Product NDC (as listed)58264-1014Labeler and product segments. Claims need a package NDC.

Product NDC at billing width58264-1014Add 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
58264-1014-1	58264101401	29.57 mL in 1 BOTTLE, GLASS (58264-1014-1)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): D14
Generic name (nonproprietary): zincum valerianicum, ignatia amara, chamomilla vulgaris, coffea cruda, kali bromatum, eschscholtzia californica, humulus lupulus, passiflora incarnata, valeriana officinalis, avena sativa
Active ingredients: Avena sativa whole — 1 [hp_X]/mLValeriana officinalis whole — 1 [hp_X]/mLHumulus lupulus whole — 2 [hp_X]/mLArabica coffee bean — 4 [hp_X]/mLStrychnos ignatii whole — 6 [hp_X]/mLZinc valerate dihydrate — 9 [hp_X]/mLChamomile — 4 [hp_X]/mLEschscholzia californica — 2 [hp_X]/mLPassiflora incarnata whole — 2 [hp_X]/mLPotassium bromide — 3 [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, 2027
Other FDA classes: Allergens (Chemical structure)Cell-mediated Immunity (Physiologic effect)Dietary Proteins (Chemical structure)Increased Histamine Release (Physiologic effect)Plant Proteins (Chemical structure)Seed Storage Proteins (Chemical structure)
Identifiers: Product ID 58264-1014_4baa48bc-4b31-969d-e063-6394a90ad1d6SPL ID 4baa48bc-4b31-969d-e063-6394a90ad1d6SPL set ID 4096bbed-b752-4082-a07c-79fc497fb8ccUNII 5P8D0Z74RG, FP6O7F1X9R, 912A6Q1N4A, 3SW678MX72, 6YSJ329777, MN0RX54EQA, FGL3685T2X, 9315HN272X, R48E2W2LMO, OSD78555ZM
Pharmacologic class: Non-Standardized Food Allergenic Extract; Non-Standardized Plant Allergenic Extract

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

N458264101401 followed by a unit qualifier and the quantity

Package 58264-1014-01. 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 Feb 25, 2026.

Indications (excerpt from the label)

INDICATIONS Insomnia and various disturbances of sleep.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)