What is NDC 62106-1101?

62106-1101 is the product NDC for Unda 2, Berberis vulgaris root bark 4 [hp_X]/20mL + 7 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 2 (Petroselinum sativum, Rhamnus frangula, Thlaspi bursa-pastoris, Juniperus communis, Asparagus officinalis, Berberis vulgaris, Genista tinctoria, Argentum metallicum).

What is the active ingredient?

Berberis vulgaris root bark, Petroselinum crispum, Asparagus, Frangula alnus bark, Capsella bursa-pastoris, Silver, Genista tinctoria, Juniper berry.

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 2?

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 2 NDC 62106-1101 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)62106-1101Labeler and product segments. Claims need a package NDC.

Product NDC at billing width62106-1101Add 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
62106-1101-8	62106110108	1 BOTTLE, GLASS in 1 CARTON (62106-1101-8) / 20 mL in 1 BOTTLE, GLASSMarketed from May 26, 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 2
Generic name (nonproprietary): petroselinum sativum, rhamnus frangula, thlaspi bursa-pastoris, juniperus communis, asparagus officinalis, berberis vulgaris, genista tinctoria, argentum metallicum
Active ingredients: Berberis vulgaris root bark — 4 [hp_X]/20mLPetroselinum crispum — 4 [hp_X]/20mLAsparagus — 4 [hp_X]/20mLFrangula alnus bark — 4 [hp_X]/20mLCapsella bursa-pastoris — 4 [hp_X]/20mLSilver — 12 [hp_X]/20mLGenista tinctoria — 4 [hp_X]/20mLJuniper berry — 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: May 26, 2015
Listing expires: Dec 31, 2026
Other FDA classes: Allergens (Chemical structure)Allergens (Chemical structure)Cell-mediated Immunity (Physiologic effect)Cell-mediated Immunity (Physiologic effect)Dietary Proteins (Chemical structure)Dietary Proteins (Chemical structure)Food Additives (Chemical structure)Increased Histamine Release (Physiologic effect)Increased Histamine Release (Physiologic effect)Plant Proteins (Chemical structure)Vegetable Proteins (Chemical structure)
Identifiers: Product ID 62106-1101_ebe194aa-984d-8373-e053-2995a90ae03eSPL ID ebe194aa-984d-8373-e053-2995a90ae03eSPL set ID 079c945e-7853-3410-e054-00144ff88e88UNII 79M2M2UDA9, O84B5194RL, CLF5YFS11O, 1WZA4Y92EX, 3M4G523W1G, X621621QQV, 1TH8Q20J0U, V5VD430YW9, AK7JF626KX, W0X9457M59, JWF5YAW3QW, Z1EJP3037Z, 6D74QW4H67, S2D77IH61R, W2FH8O2BBE, 52JDS841PX, G3QC02NIE6, 269XH13919, I76KB35JEV, 8L72OKJ7II, 2P299V784P, B4R1EZ1R1D, YF70189L0N, 79Y1949PYO
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

N462106110108 followed by a unit qualifier and the quantity

Package 62106-1101-08. 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 Oct 25, 2022.

Indications (excerpt from the label)

Uses For the temporary relief of symptoms associated with minor fever. 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 62106-1101

What is NDC 62106-1101?: 62106-1101 is the product NDC for Unda 2, Berberis vulgaris root bark 4 [hp_X]/20mL + 7 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 2 (Petroselinum sativum, Rhamnus frangula, Thlaspi bursa-pastoris, Juniperus communis, Asparagus officinalis, Berberis vulgaris, Genista tinctoria, Argentum metallicum).
What is the active ingredient?: Berberis vulgaris root bark, Petroselinum crispum, Asparagus, Frangula alnus bark, Capsella bursa-pastoris, Silver, Genista tinctoria, Juniper berry.
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 2?: 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.