NDC codes

FDA NDC Directory
Product NDC (as listed)62106-1112Labeler and product segments. Claims need a package NDC.
Product NDC at billing width62106-1112Add 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
62106-1112-8621061112081 BOTTLE, GLASS in 1 BOX (62106-1112-8) / 20 mL in 1 BOTTLE, GLASSMarketed from Dec 17, 2014

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)
Unda 13
Generic name (nonproprietary)
boldo leaf, ricinus communis seed, combretum raimbaultii leaf, jateorhiza palmata root, argentum metallicum
Active ingredients
Silver — 12 [hp_X]/20mLPeumus boldus leaf — 4 [hp_X]/20mLRicinus communis seed — 4 [hp_X]/20mLCombretum micranthum leaf — 4 [hp_X]/20mLJateorhiza calumba root — 4 [hp_X]/20mL
Dosage form
Liquid
Route
Oral
Labeler
Seroyal USANDC labeler code 62106
Product type
Over-the-counter drug
Marketing category
Unapproved homeopathic
Marketing start
Listing expires
Identifiers
Product ID 62106-1112_ecfac63b-c330-06d2-e053-2995a90aecbaSPL ID ecfac63b-c330-06d2-e053-2995a90aecbaSPL set ID 0a6be318-a469-385b-e054-00144ff8d46cUNII 3M4G523W1G, Q4EWM09M3O, 7EK4SFN1TX, 8502S3Z5N1, V36I2B8LD5

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

N462106111208 followed by a unit qualifier and the quantity

Package 62106-1112-08. 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 the temporary relief of symptoms associated with digestive upset. Directions Adults and adolescents (12 years and older) Take 5 drops three times daily or as recommended by your healthcare practitioner. Children (under 12 years) Take under the direction of your healthcare practitioner.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 62106-1112

What is NDC 62106-1112?
62106-1112 is the product NDC for Unda 13, Silver 12 [hp_X]/20mL + 4 more ingredients liquid, listed with the FDA by Seroyal USA. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Unda 13 (Boldo Leaf, Ricinus communis Seed, Combretum raimbaultii Leaf, Jateorhiza palmata Root, Argentum metallicum).
What is the active ingredient?
Silver, Peumus boldus leaf, Ricinus communis seed, Combretum micranthum leaf, Jateorhiza calumba root.
Who is the labeler?
Seroyal USA, NDC labeler code 62106. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Unda 13?
None: this is the only finished product listed under this name.
Is there a related HCPCS / J-code?
Not in Med-Code's curated HCPCS directory. See Billing references above.

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