Attention Deficit Severe Drops 2147 NDC 63083-2147

NDC codes

FDA NDC Directory

Product NDC (as listed)63083-2147Labeler and product segments. Claims need a package NDC.

Product NDC at billing width63083-2147Add 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
63083-2147-2	63083214702	59 mL in 1 BOTTLE, DROPPER (63083-2147-2)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): Attention Deficit Severe Drops 2147Suffix: 2147
Generic name (nonproprietary): attention deficit severe drops
Active ingredients: .gamma.-aminobutyric acid — 3 [hp_X]/59mLGinkgo — 3 [hp_X]/59mLBos taurus brain — 6 [hp_X]/59mLBos taurus hypothalamus — 6 [hp_X]/59mLBeef kidney — 6 [hp_X]/59mLBeef liver — 6 [hp_X]/59mLBos taurus pancreas — 6 [hp_X]/59mLSus scrofa pineal gland — 6 [hp_X]/59mLSilver nitrate — 30 [hp_X]/59mLCoffea arabica seed, Roasted — 30 [hp_X]/59mLLycopodium clavatum spore — 30 [hp_X]/59mLAmaryllis belladonna whole — 60 [hp_X]/59mLPhosphorus — 60 [hp_X]/59mLAmbergris — 60 [hp_X]/59mLBarium carbonate — 60 [hp_X]/59mLBarium chloride dihydrate — 60 [hp_X]/59mLBufo bufo cutaneous gland — 60 [hp_X]/59mLHyoscyamus niger — 60 [hp_X]/59mLGonorrheal urethral secretion human — 60 [hp_X]/59mLDatura stramonium — 60 [hp_X]/59mLLycosa tarantula — 60 [hp_X]/59mLThuja occidentalis leaf — 60 [hp_X]/59mLBovine tuberculin — 60 [hp_X]/59mLVeratrum album root — 60 [hp_X]/59mLInsulin glulisine — 60 [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: Allergens (Chemical structure)Cell-mediated Immunity (Physiologic effect)Dietary Proteins (Chemical structure)Increased Histamine Release (Physiologic effect)Insulin (Chemical/Ingredient)Meat Proteins (EXT)
Identifiers: Product ID 63083-2147_964caa36-9f97-451e-bbc2-b425492baa15SPL ID 964caa36-9f97-451e-bbc2-b425492baa15SPL set ID cd45062c-f3b1-439f-a559-3582d5c62173UNII 2ACZ6IPC6I, 19FUJ2C58T, A1YEE2DB8Z, S6G2NLH4Y7, 5HOC10FSIC, W8N8R55022, 1M529TNT1D, 050QZ2EDK7, 95IT3W8JZE, 9H58JRT35E, C88X29Y479, 11B89M58UN, 27YLU75U4W, XTC0D02P6C, 6P669D8HQ8, EL5GJ3U77E, Q59QU6N72Q, 4WRK2153H3, 9BZG9E3I8F, G6W4F0V8Z3, 86M454L2TT, 0T0DQN8786, HKD62G79N5, QNS6W5US1Z, 7XIY785AZD
Pharmacologic class: Insulin Analog; 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

N463083214702 followed by a unit qualifier and the quantity

Package 63083-2147-02. 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 moderate or more severe excitability, fidgeting, or lack of restraint or focus.*

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)