What is NDC 63083-2007?

63083-2007 is the product NDC for Anti-Smoking I Drops 2007 (anti-smoking i drops), Tobacco leaf 4 [hp_X]/59mL + 8 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?

Anti-Smoking I Drops 2007 (Anti-Smoking I Drops).

What is the active ingredient?

Tobacco leaf, Sus scrofa adrenal gland, Lobelia cardinalis whole, Beef lung, Nicotine, Beta-endorphin human, Coffea arabica seed, Roasted, Strychnos nux-vomica seed, Sucrose.

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 Anti-Smoking I Drops 2007?

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.

Anti-Smoking I Drops 2007 NDC 63083-2007

NDC codes

FDA NDC Directory

Product NDC (as listed)63083-2007Labeler and product segments. Claims need a package NDC.

Product NDC at billing width63083-2007Add 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
63083-2007-2	6308320070263083200702	59 mL in 1 BOTTLE, DROPPER (63083-2007-2)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): Anti-Smoking I Drops 2007Suffix: 2007
Generic name (nonproprietary): anti-smoking i drops
Active ingredients: Tobacco leaf — 4 [hp_X]/59mLSus scrofa adrenal gland — 6 [hp_X]/59mLLobelia cardinalis whole — 6 [hp_X]/59mLBeef lung — 6 [hp_X]/59mLNicotine — 6 [hp_X]/59mLBeta-endorphin human — 6 [hp_X]/59mLCoffea arabica seed, Roasted — 6 [hp_X]/59mLStrychnos nux-vomica seed — 12 [hp_X]/59mLSucrose — 16 [hp_X]/59mL
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)Allergens (Chemical structure)Cell-mediated Immunity (Physiologic effect)Cell-mediated Immunity (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased IgG Production (Physiologic effect)Increased IgG Production (Physiologic effect)Nicotine (Chemical structure)Plant Proteins (Chemical structure)Plant Proteins (Chemical structure)Seed Storage Proteins (Chemical structure)
Identifiers: Product ID 63083-2007_b9687c56-81f4-4f42-bbc8-6fc70eab217dSPL ID b9687c56-81f4-4f42-bbc8-6fc70eab217dSPL set ID 1c6b5b98-971d-442a-b9eb-37f65409a521UNII 6YR2608RSU, 398IYQ16YV, GT0PJ8MB5R, 2I1RTO1MBR, 6M3C89ZY6R, 3S51P4W3XQ, 9H58JRT35E, 269XH13919, C151H8M554
Pharmacologic class: Cholinergic Nicotinic Agonist; Non-Standardized Plant 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

N463083200702 followed by a unit qualifier and the quantity

Package 63083-2007-02. 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 Temporarily reduces cravings while attempting to quit smoking.*

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 63083-2007

What is NDC 63083-2007?: 63083-2007 is the product NDC for Anti-Smoking I Drops 2007 (anti-smoking i drops), Tobacco leaf 4 [hp_X]/59mL + 8 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?: Anti-Smoking I Drops 2007 (Anti-Smoking I Drops).
What is the active ingredient?: Tobacco leaf, Sus scrofa adrenal gland, Lobelia cardinalis whole, Beef lung, Nicotine, Beta-endorphin human, Coffea arabica seed, Roasted, Strychnos nux-vomica seed, Sucrose.
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 Anti-Smoking I Drops 2007?: 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.

Anti-Smoking I Drops 2007 (Anti-smoking i drops) NDC 63083-2007