Bridged Chlorinated Ring Combination 9313 NDC 63083-9313

NDC codes

FDA NDC Directory

Product NDC (as listed)63083-9313Labeler and product segments. Claims need a package NDC.

Product NDC at billing width63083-9313Add 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
63083-9313-1	63083931301	29.5 mL in 1 BOTTLE, DROPPER (63083-9313-1)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 Chlorinated Ring Combination 9313Suffix: 9313
Generic name (nonproprietary): bridged chlorinated ring combination
Active ingredients: Black cohosh — 3 [hp_X]/29.5mLGelsemium sempervirens root — 3 [hp_X]/29.5mLBerberis vulgaris root bark — 10 [hp_X]/29.5mLChelidonium majus whole — 10 [hp_X]/29.5mLParaquat dichloride — 12 [hp_X]/29.5mLThuja occidentalis leaf — 12 [hp_X]/29.5mLDichlorvos — 16 [hp_X]/29.5mL
Dosage form: Liquid
Route: Oral
Labeler: Professional Complementary Health Formulas
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Aug 15, 1984
Listing expires: Dec 31, 2027
Identifiers: Product ID 63083-9313_4147062f-b9e2-4d0d-b219-80bfbfe076aaSPL ID 4147062f-b9e2-4d0d-b219-80bfbfe076aaSPL set ID aef0383e-756d-4239-a293-48d6cdcd6a1dUNII K73E24S6X9, 639KR60Q1Q, 1TH8Q20J0U, 7E889U5RNN, 2KZ83GSS73, 0T0DQN8786, 7U370BPS14

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

N463083931301 followed by a unit qualifier and the quantity

Package 63083-9313-01. 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 Jan 8, 2026.

Indications (excerpt from the label)

INDICATIONS For the temporary relief of upper respiratory irritation, minor sore throat, stomach discomfort, vomiting, diarrhea, or weakness.*

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)