NDC codes

FDA NDC Directory
Product NDC (as listed)62106-0625Labeler and product segments. Claims need a package NDC.
Product NDC at billing width62106-0625Add 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
62106-0625-062106062500621060625001 BOTTLE, GLASS in 1 CARTON (62106-0625-0) / 30 mL in 1 BOTTLE, GLASSMarketed from Dec 14, 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)
Hki
Generic name (nonproprietary)
atropinum sulphuricum, benzoicum acidum, berberis vulgaris, calcarea carbonica, colocynthis, coccus cacti, lapis albus, lithium carbonicum, lycopodium clavatum, oryctolagus cuniculus kidney, rubia tinctorum, sarsaparilla, urtica urens
Active ingredients
Atropine sulfate — 6 [hp_X]/30mLOyster shell calcium carbonate, Crude — 12 [hp_X]/30mLCitrullus colocynthis fruit pulp — 6 [hp_X]/30mLLycopodium clavatum spore — 5 [hp_X]/30mLOryctolagus cuniculus kidney — 10 [hp_X]/30mLSarsaparilla — 1 [hp_X]/30mLCalcium hexafluorosilicate — 12 [hp_C]/30mLBenzoic acid — 6 [hp_X]/30mLProtortonia cacti — 5 [hp_X]/30mLLithium carbonate — 6 [hp_X]/30mLRubia tinctorum root — 4 [hp_X]/30mLUrtica urens — 1 [hp_X]/30mLBerberis vulgaris root bark — 5 [hp_X]/30mL
Dosage form
Liquid
Route
Sublingual
Labeler
Seroyal USANDC labeler code 62106
Product type
Over-the-counter drug
Marketing category
Unapproved homeopathic
Marketing start
Listing expires
Other FDA classes
Ammonium Ion Binding Activity (Mechanism)Cholinergic Antagonists (Mechanism)Cholinergic Muscarinic Antagonists (Mechanism)
Identifiers
Product ID 62106-0625_f38e873c-cc3c-f701-e053-2a95a90af213SPL ID f38e873c-cc3c-f701-e053-2a95a90af213SPL set ID 26e048f5-8e87-51e6-e054-00144ff88e88UNII 03J5ZE7KA5, 2E32821G6I, 23H32AOH17, C88X29Y479, 482QQ7H44Q, 2H1576D5WG, 2NVP93XVQ3, 8SKN0B0MIM, LZB7TFX1LT, 2BMD2GNA4V, 0SVP95L23G, IHN2NQ5OF9, 1TH8Q20J0UUPC 0883196138500
Pharmacologic class
Anticholinergic; Cholinergic Muscarinic Antagonist; Mood Stabilizer; Nitrogen Binding Agent

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. Sublingual products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N462106062500 followed by a unit qualifier and the quantity

Package 62106-0625-00. 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 healthy kidney and urinary tract functions. 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 62106-0625

What is NDC 62106-0625?
62106-0625 is the product NDC for Hki, Atropine sulfate 6 [hp_X]/30mL + 12 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?
Hki (Atropinum sulphuricum, Benzoicum acidum, Berberis vulgaris, Calcarea carbonica, Colocynthis, Coccus cacti, Lapis albus, Lithium carbonicum, Lycopodium clavatum, Oryctolagus cuniculus kidney, Rubia tinctorum, Sarsaparilla, Urtica urens).
What is the active ingredient?
Atropine sulfate, Oyster shell calcium carbonate, Crude, Citrullus colocynthis fruit pulp, Lycopodium clavatum spore, Oryctolagus cuniculus kidney, Sarsaparilla, Calcium hexafluorosilicate, Benzoic acid, Protortonia cacti, Lithium carbonate, Rubia tinctorum root, Urtica urens, Berberis vulgaris root bark.
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 Hki?
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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