What is NDC 62106-1158?

62106-1158 is the product NDC for Unda 226, Peumus boldus leaf 6 [hp_X]/20mL + 5 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 226 (Urtica dioica, Berberis vulgaris, Boldo, Juniperus communis, Aloe socotrina, Chelidonium majus).

What is the active ingredient?

Peumus boldus leaf, Urtica dioica, Berberis vulgaris root bark, Juniper berry, Aloe, Chelidonium majus.

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 226?

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.

Unda 226 NDC 62106-1158 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)62106-1158Labeler and product segments. Claims need a package NDC.

Product NDC at billing width62106-1158Add 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
62106-1158-8	6210611580862106115808	1 BOTTLE, GLASS in 1 CARTON (62106-1158-8) / 20 mL in 1 BOTTLE, GLASSMarketed from Jun 2, 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 226
Generic name (nonproprietary): urtica dioica, berberis vulgaris, boldo, juniperus communis, aloe socotrina, chelidonium majus
Active ingredients: Peumus boldus leaf — 6 [hp_X]/20mLUrtica dioica — 6 [hp_X]/20mLBerberis vulgaris root bark — 6 [hp_X]/20mLJuniper berry — 6 [hp_X]/20mLAloe — 6 [hp_X]/20mLChelidonium majus — 6 [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: Jun 2, 2015
Listing expires: Dec 31, 2026
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 62106-1158_c73082d2-60ff-4cbf-e053-2a95a90a8f9bSPL ID c73082d2-60ff-4cbf-e053-2a95a90a8f9bSPL set ID 1789ed21-3bc9-3b86-e054-00144ff88e88UNII 710FLW4U46, 7D28M9SL9B, Q35465A1MA, IDB0NAZ6AI, 4817H7M565, E55SMD6DA8, 789U1901C5, IH3063S9MY, 75O014T1HG, 7114SV0MYK, BI896CKT6B, V36I2B8LD5, 5405K23S50, 3M4G523W1G, ZW3Z11D0JV, 7E889U5RNN, 1L0VKZ185E, N20HL7Q941, C88X29Y479, 6177A89GA2, 2788Z9758H, Q4EWM09M3O, 79Y1949PYO, 7H0QTZ446K, 9Q24RAI43V, O84B5194RL, W0X9457M59, 1TH8Q20J0U, T7J046YI2B, V5VD430YW9, S546YLW6E6, 2FXJ6SW4PK, Q21UUL2105
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

N462106115808 followed by a unit qualifier and the quantity

Package 62106-1158-08. 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 Jul 15, 2021.

Indications (excerpt from the label)

Uses For the temporary relief of symptoms associated with common colds. 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 62106-1158

What is NDC 62106-1158?: 62106-1158 is the product NDC for Unda 226, Peumus boldus leaf 6 [hp_X]/20mL + 5 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 226 (Urtica dioica, Berberis vulgaris, Boldo, Juniperus communis, Aloe socotrina, Chelidonium majus).
What is the active ingredient?: Peumus boldus leaf, Urtica dioica, Berberis vulgaris root bark, Juniper berry, Aloe, Chelidonium majus.
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 226?: 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.