Over-the-counter drug · UNAPPROVED HOMEOPATHIC
Unda 700 (Berberis vulgaris, calcarea fluorica) NDC 62106-1171
Berberis vulgaris root bark 4 [hp_X]/20mL; Calcium fluoride 12 [hp_X]/20mL · Liquid · Oral · Seroyal USA
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 62106-1171-8 | 6210611710862106117108 | 1 BOTTLE, GLASS in 1 CARTON (62106-1171-8) / 20 mL in 1 BOTTLE, GLASSMarketed from Sep 23, 2015 |
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 700
- Generic name (nonproprietary)
- berberis vulgaris, calcarea fluorica
- Active ingredients
- Berberis vulgaris root bark — 4 [hp_X]/20mLCalcium fluoride — 12 [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 62106-1171_c733ec78-5b43-7a7c-e053-2995a90a2f9aSPL ID c733ec78-5b43-7a7c-e053-2995a90a2f9aSPL set ID 206a5750-2025-205e-e054-00144ff8d46cUNII 75O014T1HG, 046Y1357I6, IDB0NAZ6AI, M7T6H7D4IF, 1TH8Q20J0U, O3B55K4YKI, DTN01M69SN, YQ2S06L8S9, Q1RGP4UB73UPC 0883196304608
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
N462106117108followed by a unit qualifier and the quantityPackage 62106-1171-08. 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 relief of symptoms associated with sore throat. 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.
About NDC 62106-1171
- What is NDC 62106-1171?
- 62106-1171 is the product NDC for Unda 700, Berberis vulgaris root bark 4 [hp_X]/20mL; Calcium fluoride 12 [hp_X]/20mL 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 700 (Berberis vulgaris, Calcarea fluorica).
- What is the active ingredient?
- Berberis vulgaris root bark, Calcium fluoride.
- 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 700?
- 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.