NDC codes

FDA NDC Directory
Product NDC (as listed)60986-1008Labeler and product segments. Claims need a package NDC.
Product NDC at billing width60986-1008Add 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
60986-1008-36098610080350 mL in 1 BOTTLE, GLASS (60986-1008-3)Marketed from Feb 27, 2018
60986-1008-460986100804100 mL in 1 BOTTLE, GLASS (60986-1008-4)Marketed from Feb 27, 2018

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)
Cholenest
Generic name (nonproprietary)
rhamnus purshiana, carduus marianus, taraxacum officinale, chelidonium majus, leptandra virginica, myrica cerifera, berberis vulgaris, natrum sulphuricum, magnesia phosphorica, cuprum metallicum
Active ingredients
Frangula purshiana bark — 1 [hp_X]/100mLSilybum marianum seed — 1 [hp_X]/100mLTaraxacum officinale — 1 [hp_X]/100mLChelidonium majus — 1 [hp_X]/100mLVeronicastrum virginicum root — 2 [hp_X]/100mLMorella cerifera root bark — 2 [hp_X]/100mLBerberis vulgaris root bark — 2 [hp_X]/100mLSodium sulfate — 6 [hp_X]/100mLMagnesium phosphate, Dibasic trihydrate — 8 [hp_X]/100mLCopper — 8 [hp_X]/100mL
Dosage form
Liquid
Route
Oral
Product type
Over-the-counter drug
Marketing category
Unapproved homeopathic
Marketing start
Listing expires
Other FDA classes
Copper (Chemical structure)Decreased Embryonic Implantation (Physiologic effect)Decreased Sperm Motility (Physiologic effect)Increased Large Intestinal Motility (Physiologic effect)Increased Large Intestinal Motility (Physiologic effect)Inhibit Ovum Fertilization (Physiologic effect)Inhibition Large Intestine Fluid/Electrolyte Absorption (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)Osmotic Activity (Mechanism)Stimulation Large Intestine Fluid/Electrolyte Secretion (Physiologic effect)
Identifiers
Product ID 60986-1008_483c66da-6d99-08e2-e063-6294a90aeb8bSPL ID 483c66da-6d99-08e2-e063-6294a90aeb8bSPL set ID 4b89ffcb-318b-416d-b13c-19fb94c2af70UNII 4VBP01X99F, U946SH95EE, 39981FM375, 7E889U5RNN, M2O62YTN42, S46HJ3710D, 1TH8Q20J0U, 0YPR65R21J, HF539G9L3Q, 789U1901C5
Pharmacologic class
Calculi Dissolution Agent; Copper-containing Intrauterine Device; 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

N460986100803 followed by a unit qualifier and the quantity

Package 60986-1008-03. 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)

Suggested use Adults: 30-40 drops in tepid water 3 times daily before meals. Children, 10 drops in tepid water 3 times daily before meals.

Excerpt only. Read the full label for complete information.

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