NDC codes

FDA NDC Directory
Product NDC (as listed)63479-0112Labeler and product segments. Claims need a package NDC.
Product NDC at billing width63479-0112Add 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 NDC11-digit (billing)PackageCopy
63479-0112-16347901120130 mL in 1 BOTTLE, GLASS (63479-0112-1)Marketed from Oct 15, 1998

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)
A12 Dtx-KidneySuffix: DTX-KIDNEY
Generic name (nonproprietary)
apis mellifica, berberis vulgaris, betula pubescens bark, betula verrucosa leaf, bos taurus kidney, bos taurus urinary bladder, citricum acidum, citrus limonum, fagus sylvestris flower bud, natrum muriaticum, petroselinum sativum, quercus robur flower bud, sinusitisinum, solidago virgaurea
Active ingredients
Petroselinum crispum — 2 [hp_X]/mLSolidago virgaurea flowering top — 1 [hp_X]/mLBetula pubescens bark — 3 [hp_X]/mLBetula pendula leaf — 1 [hp_X]/mLBeef kidney — 7 [hp_C]/mLFagus sylvatica flower bud — 1 [hp_X]/mLBerberis vulgaris root bark — 9 [hp_X]/mLBos taurus urinary bladder — 7 [hp_C]/mLAnhydrous citric acid — 12 [hp_X]/mLLemon juice — 3 [hp_X]/mLQuercus robur flower bud — 1 [hp_X]/mLSinusitisinum — 7 [hp_C]/mLApis mellifera — 6 [hp_X]/mLSodium chloride — 15 [hp_X]/mL
Dosage form
Solution/ drops
Route
Sublingual
Product type
Over-the-counter drug
Marketing category
Unapproved homeopathic
Marketing start
Listing expires
Other FDA classes
Acidifying Activity (Mechanism)Allergens (Chemical structure)Bee Venoms (Chemical structure)Calcium Chelating Activity (Mechanism)Cell-mediated Immunity (Physiologic effect)Decreased Coagulation Factor Activity (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased IgG Production (Physiologic effect)Increased Large Intestinal Motility (Physiologic effect)Inhibition Large Intestine Fluid/Electrolyte Absorption (Physiologic effect)Osmotic Activity (Mechanism)
Identifiers
Product ID 63479-0112_0e764c29-02d9-6485-e063-6394a90a6a45SPL ID 0e764c29-02d9-6485-e063-6394a90a6a45SPL set ID bf52e26f-aa27-87ca-e053-2995a90a23e7UNII 1WZA4Y92EX, 5405K23S50, 3R504894L9, 5HW39H9KDH, 5HOC10FSIC, 6D5V13045W, 1TH8Q20J0U, 0SLJ2C1IHA, XF417D3PSL, AGN709ANTJ, VC5I578BE3, B575563DM5, 7S82P3R43Z, 451W47IQ8X
Pharmacologic class
Anti-coagulant; Calculi Dissolution Agent; Osmotic Laxative; Standardized Insect Venom 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

N463479011201 followed by a unit qualifier and the quantity

Package 63479-0112-01. 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 .

Indications (excerpt from the label)

Uses: For temporary relief of minor: urinary discomfort* headache* vertigo* water retention* backache* *Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

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