NDC codes

FDA NDC Directory
Product NDC (as listed)63083-9312Labeler and product segments. Claims need a package NDC.
Product NDC at billing width63083-9312Add 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
63083-9312-16308393120129.5 mL in 1 BOTTLE, DROPPER (63083-9312-1)Marketed from Aug 15, 1985

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)
Bridged Phenyl Combination 9312Suffix: 9312
Generic name (nonproprietary)
bridged phenyl combination
Active ingredients
Berberis vulgaris root bark — 10 [hp_X]/29.5mLChelidonium majus whole — 10 [hp_X]/29.5mLBos taurus bile — 10 [hp_X]/29.5mLProxifezone — 12 [hp_X]/29.5mLPropham — 12 [hp_X]/29.5mLSodium — 12 [hp_X]/29.5mL3'-methylphthalanilic acid — 16 [hp_X]/29.5mL
Dosage form
Liquid
Route
Oral
Product type
Over-the-counter drug
Marketing category
Unapproved homeopathic
Marketing start
Listing expires
Identifiers
Product ID 63083-9312_c4c43e2f-836c-46d8-ae18-22ed57618c38SPL ID c4c43e2f-836c-46d8-ae18-22ed57618c38SPL set ID 151c2748-a1dd-4406-a3d4-9d7baf98777dUNII 1TH8Q20J0U, 7E889U5RNN, ET3651ZLOU, 005MKH0F6D, Y647G714RY, 9NEZ333N27, 3R15BUY339

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

N463083931201 followed by a unit qualifier and the quantity

Package 63083-9312-01. 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)

INDICATIONS For the temporary relief of occasional headache, nausea or vomiting, cough, minor sore throat, or skin, eye, or upper respiratory irritation.*

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

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