Opsin I 6014 (opsin i) NDC 63083-6014

NDC codes

FDA NDC Directory

Product NDC (as listed)63083-6014Labeler and product segments. Claims need a package NDC.

Product NDC at billing width63083-6014Add 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
63083-6014-2	63083601402	59 mL in 1 BOTTLE, DROPPER (63083-6014-2)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): Opsin I 6014Suffix: 6014
Generic name (nonproprietary): opsin i
Active ingredients: Epinephrine — 6 [hp_X]/59mLSilver nitrate — 6 [hp_X]/59mLArsenic trioxide — 6 [hp_X]/59mLActivated charcoal — 6 [hp_X]/59mLHydrangea arborescens root — 6 [hp_X]/59mLLiquid petroleum — 6 [hp_X]/59mLAcetaldehyde — 12 [hp_X]/59mLCoumarin — 12 [hp_X]/59mLGallic acid monohydrate — 12 [hp_X]/59mLHistamine dihydrochloride — 12 [hp_X]/59mLIndole-3-carbinol — 12 [hp_X]/59mLYeast mannan — 12 [hp_X]/59mLRutin — 12 [hp_X]/59mLDeoxymutaaspergillic acid — 30 [hp_X]/59mL
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
Other FDA classes: Adrenergic alpha-Agonists (Mechanism)Adrenergic beta-Agonists (Mechanism)Catecholamines (Chemical structure)
Identifiers: Product ID 63083-6014_bca11e36-d24b-43e5-bded-e202480df00fSPL ID bca11e36-d24b-43e5-bded-e202480df00fSPL set ID ac4185b4-7b9b-4608-9157-d8be86582ff8UNII YKH834O4BH, 95IT3W8JZE, S7V92P67HO, 2P3VWU3H10, SFK828Q2DE, 6ZAE7X688J, GO1N1ZPR3B, A4VZ22K1WT, 48339473OT, 3POA0Q644U, C11E72455F, 91R887N59P, 5G06TVY3R7, 0C9LJ2USYB
Pharmacologic class: Catecholamine; alpha-Adrenergic Agonist; beta-Adrenergic Agonist

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

N463083601402 followed by a unit qualifier and the quantity

Package 63083-6014-02. 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 gas, bloating, diarrhea, runny nose, sneezing, itching of the nose or throat, and itchy or watery eyes due to sensitivity to food allergens or autotoxins.*

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)