Over-the-counter drug · UNAPPROVED HOMEOPATHIC
Unda 43 NDC 62106-1142
Equisetum arvense top 4 [hp_X]/20mL + 6 more ingredients · Liquid · Oral · Seroyal USA
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 62106-1142-8 | 62106114208 | 1 BOTTLE, GLASS in 1 CARTON (62106-1142-8) / 20 mL in 1 BOTTLE, GLASSMarketed from Sep 22, 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 43
- Generic name (nonproprietary)
- aluminium metallicum, asperula odorata, equisetum arvense, jateorhiza palmata, marrubium vulgare, ocimum basilicum, stannum metallicum
- Active ingredients
- Equisetum arvense top — 4 [hp_X]/20mLJateorhiza calumba root — 4 [hp_X]/20mLGalium odoratum — 4 [hp_X]/20mLMarrubium vulgare — 4 [hp_X]/20mLBasil — 4 [hp_X]/20mLTin — 12 [hp_X]/20mLAluminum — 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
- Other FDA classes
- Allergens (Chemical structure)Cell-mediated Immunity (Physiologic effect)Dietary Proteins (Chemical structure)Food Additives (Chemical structure)Increased Histamine Release (Physiologic effect)Plant Proteins (Chemical structure)
- Identifiers
- Product ID 62106-1142_ed10aff6-7a4c-4115-e053-2995a90a9d1aSPL ID ed10aff6-7a4c-4115-e053-2995a90a9d1aSPL set ID 20569964-d505-03e2-e054-00144ff8d46cUNII JWF5YAW3QW, 7A72MUN24Z, CPD4NFA903, V36I2B8LD5, 387GMG9FH5, 1DP6Y6B65Z, F84709P2XV, MUE8Y11327, 2U0KZP0FDW, N8C4A9A49H, IJ67X351P9, 79Y1949PYO, 9IT35J3UV3, 8L72OKJ7II
- 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. Oral products like this are usually dispensed by a pharmacy and billed by NDC.
- NDC on a medical claim
N462106114208followed by a unit qualifier and the quantityPackage 62106-1142-08. 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)
UsesUses For the temporary relief of symptoms associated with dizziness, mental fatigue and nervousness. 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 62106-1142
- What is NDC 62106-1142?
- 62106-1142 is the product NDC for Unda 43, Equisetum arvense top 4 [hp_X]/20mL + 6 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 43 (Aluminium metallicum, Asperula odorata, Equisetum arvense, Jateorhiza palmata, Marrubium vulgare, Ocimum basilicum, Stannum metallicum).
- What is the active ingredient?
- Equisetum arvense top, Jateorhiza calumba root, Galium odoratum, Marrubium vulgare, Basil, Tin, Aluminum.
- 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 43?
- 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.