Dna Rna NDC 43853-0014

NDC codes

FDA NDC Directory

Product NDC (as listed)43853-0014Labeler and product segments. Claims need a package NDC.

Product NDC at billing width43853-0014Add 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
43853-0014-1	43853001401	30 mL in 1 BOTTLE, SPRAY (43853-0014-1)Marketed from Nov 23, 2016

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): Dna Rna
Generic name (nonproprietary): arnica montana, avena sativa, damiana, dna, hypophysis suis, oleum animale, panax ginseng, rna, thuja occidentalis
Active ingredients: Arnica montana — 6 [hp_X]/mLAvena sativa flowering top — 3 [hp_X]/mLTurnera diffusa leafy twig — 3 [hp_X]/mLHerring sperm DNA — 9 [hp_X]/mLSus scrofa pituitary gland — 5 [hp_C]/mLCervus elaphus horn oil — 6 [hp_X]/mLAsian ginseng — 3 [hp_X]/mLSaccharomyces cerevisiae RNA — 9 [hp_X]/mLThuja occidentalis leafy twig — 6 [hp_X]/mL
Dosage form: Spray
Route: Oral
Labeler: ProBLEN
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Nov 23, 2016
Listing expires: Dec 31, 2026
Identifiers: Product ID 43853-0014_28033bb9-bd2c-4223-a7e7-b7fd11286091SPL ID 28033bb9-bd2c-4223-a7e7-b7fd11286091SPL set ID c7b5d739-2f25-4149-a6e0-efa54293604dUNII O80TY208ZW, MA9CQJ3F7F, RQ2CFA7WWJ, 51FI676N6F, L0PFEMQ1DT, 7A7G0PQI12, CUQ3A77YXI, J17GBZ5VGX, 1NT28V9397

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. Oral products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N443853001401 followed by a unit qualifier and the quantity

Package 43853-0014-01. 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 Nov 23, 2016.

Indications (excerpt from the label)

INDICATIONS: Temporarily supports symptoms of a run-down condition or advancing age. Symptoms may include: Low energy, poor muscular strength and stamina, pain and stiffness in muscles and joints, forgetfulness, inability to concentrate.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)