What is NDC 63083-3012?

63083-3012 is the product NDC for Oxy Bee Pollen Liquescence 3012 (oxy bee pollen liquescence), Bee pollen 2 [hp_X]/118mL + 10 more ingredients liquid, listed with the FDA by Professional Complementary Health Formulas. It has 1 package NDC, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

Oxy Bee Pollen Liquescence 3012 (Oxy Bee Pollen Liquescence).

What is the active ingredient?

Bee pollen, English sole, DNA-directed RNA polymerase subunit beta (M. Tuberculosis), Bitter almond, Fucus vesiculosus, Laminaria japonica, Medicago sativa whole, Royal jelly, Zinc, Pantothenic acid, Comfrey root.

Professional Complementary Health Formulas, NDC labeler code 63083. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Oxy Bee Pollen Liquescence 3012?

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.

Oxy Bee Pollen Liquescence 3012 NDC 63083-3012

NDC codes

FDA NDC Directory

Product NDC (as listed)63083-3012Labeler and product segments. Claims need a package NDC.

Product NDC at billing width63083-3012Add 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
63083-3012-4	6308330120463083301204	118 mL in 1 BOTTLE, DROPPER (63083-3012-4)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): Oxy Bee Pollen Liquescence 3012Suffix: 3012
Generic name (nonproprietary): oxy bee pollen liquescence
Active ingredients: Bee pollen — 2 [hp_X]/118mLEnglish sole — 2 [hp_X]/118mLDNA-directed RNA polymerase subunit beta (M. Tuberculosis) — 2 [hp_X]/118mLBitter almond — 3 [hp_X]/118mLFucus vesiculosus — 3 [hp_X]/118mLLaminaria japonica — 3 [hp_X]/118mLMedicago sativa whole — 3 [hp_X]/118mLRoyal jelly — 3 [hp_X]/118mLZinc — 4 [hp_X]/118mLPantothenic acid — 6 [hp_X]/118mLComfrey root — 6 [hp_X]/118mL
Dosage form: Liquid
Route: Oral
Labeler: Professional Complementary Health FormulasNDC labeler code 63083
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Aug 15, 1984
Listing expires: Dec 31, 2027
Other FDA classes: Allergens (Chemical structure)Cell-mediated Immunity (Physiologic effect)Dietary Proteins (Chemical structure)Dietary (EXT)Increased Histamine Release (Physiologic effect)
Identifiers: Product ID 63083-3012_1e7e4c97-92cf-4881-89cf-49e0e752822dSPL ID 1e7e4c97-92cf-4881-89cf-49e0e752822dSPL set ID 2d6cade7-7e1b-4859-b538-9d0ab70cccb8UNII 3729L8MA2C, 00CR8124AS, 1C627X5G1B, O65SFW8R9A, 535G2ABX9M, WE98HW412B, DJO934BRBD, L497I37F0C, J41CSQ7QDS, 19F5HK2737, M9VVZ08EKQ
Pharmacologic class: Non-Standardized Food Allergenic Extract

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

N463083301204 followed by a unit qualifier and the quantity

Package 63083-3012-04. 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 inflammation, mild pain or stiffness in joints, muscles, or surrounding tissues, irritability, poor concentration, diminished memory, fatigue, or general weakness.*

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 63083-3012

What is NDC 63083-3012?: 63083-3012 is the product NDC for Oxy Bee Pollen Liquescence 3012 (oxy bee pollen liquescence), Bee pollen 2 [hp_X]/118mL + 10 more ingredients liquid, listed with the FDA by Professional Complementary Health Formulas. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Oxy Bee Pollen Liquescence 3012 (Oxy Bee Pollen Liquescence).
What is the active ingredient?: Bee pollen, English sole, DNA-directed RNA polymerase subunit beta (M. Tuberculosis), Bitter almond, Fucus vesiculosus, Laminaria japonica, Medicago sativa whole, Royal jelly, Zinc, Pantothenic acid, Comfrey root.
Who is the labeler?: Professional Complementary Health Formulas, NDC labeler code 63083. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Oxy Bee Pollen Liquescence 3012?: 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.

Oxy Bee Pollen Liquescence 3012 (Oxy bee pollen liquescence) NDC 63083-3012