NDC codes

FDA NDC Directory
Product NDC (as listed)62106-0622Labeler and product segments. Claims need a package NDC.
Product NDC at billing width62106-0622Add 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
62106-0622-062106062200621060622001 BOTTLE, GLASS in 1 CARTON (62106-0622-0) / 30 mL in 1 BOTTLE, GLASSMarketed from Nov 25, 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)
Had
Generic name (nonproprietary)
atropinum sulphuricum, berberis vulgaris, bryonia, carduus marianus, chelidonium majus, echinacea angustifolia, lycopodium clavatum, magnesia phosphorica, oryctolagus cuniculus (rabbit) adrenal gland, oryctolagus cuniculus (rabbit) spleen, zingiber officinale (ginger) rhizome
Active ingredients
Atropine sulfate — 6 [hp_X]/30mLBerberis vulgaris root bark — 3 [hp_X]/30mLBryonia alba root — 4 [hp_X]/30mLMilk thistle — 2 [hp_X]/30mLChelidonium majus root — 3 [hp_X]/30mLEchinacea, Unspecified — 2 [hp_X]/30mLLycopodium clavatum spore — 12 [hp_X]/30mLOryctolagus cuniculus adrenal gland — 10 [hp_X]/30mLGinger — 2 [hp_X]/30mLMagnesium phosphate, Dibasic trihydrate — 6 [hp_X]/30mLOryctolagus cuniculus spleen — 10 [hp_X]/30mL
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)Cholinergic Antagonists (Mechanism)Cholinergic Muscarinic Antagonists (Mechanism)Dietary Proteins (Chemical structure)Food Additives (Chemical structure)Increased Histamine Release (Physiologic effect)Increased Large Intestinal Motility (Physiologic effect)Inhibition Large Intestine Fluid/Electrolyte Absorption (Physiologic effect)Inhibition Small Intestine Fluid/Electrolyte Absorption (Physiologic effect)Magnesium Ion Exchange Activity (Mechanism)Osmotic Activity (Mechanism)Plant Proteins (Chemical structure)Stimulation Large Intestine Fluid/Electrolyte Secretion (Physiologic effect)
Identifiers
Product ID 62106-0622_c7c0338a-9dbd-131d-e053-2a95a90a6252SPL ID c7c0338a-9dbd-131d-e053-2a95a90a6252SPL set ID 25665b4f-82ec-11be-e054-00144ff88e88UNII 03J5ZE7KA5, 1TH8Q20J0U, T7J046YI2B, U946SH95EE, FLT36UCF0N, 4N9P6CC1DX, C88X29Y479, QGY289M89Q, C5529G5JPQ, HF539G9L3Q, 01WNS05SFOUPC 0883196138807
Pharmacologic class
Anticholinergic; Calculi Dissolution Agent; Cholinergic Muscarinic Antagonist; Non-Standardized Food Allergenic Extract; Non-Standardized Plant Allergenic Extract; Osmotic Laxative

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

N462106062200 followed by a unit qualifier and the quantity

Package 62106-0622-00. 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 Helps promote and maintain natural resistance to stress and normal energy levels. Directions To be taken 20 minutes away from food. Place drops directly under the tongue or into ¼ oz of water. Adults and adolescents (12 years and older): Take 10 drops two to 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 62106-0622

What is NDC 62106-0622?
62106-0622 is the product NDC for Had, Atropine sulfate 6 [hp_X]/30mL + 10 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?
Had (Atropinum sulphuricum, Berberis vulgaris, Bryonia, Carduus marianus, Chelidonium majus, Echinacea angustifolia, Lycopodium clavatum, Magnesia phosphorica, Oryctolagus cuniculus (Rabbit) Adrenal Gland, Oryctolagus cuniculus (Rabbit) Spleen, Zingiber officinale (Ginger) Rhizome).
What is the active ingredient?
Atropine sulfate, Berberis vulgaris root bark, Bryonia alba root, Milk thistle, Chelidonium majus root, Echinacea, Unspecified, Lycopodium clavatum spore, Oryctolagus cuniculus adrenal gland, Ginger, Magnesium phosphate, Dibasic trihydrate, Oryctolagus cuniculus spleen.
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 Had?
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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