Glucoseforce HP NDC 43857-0648

NDC codes

FDA NDC Directory

Product NDC (as listed)43857-0648Labeler and product segments. Claims need a package NDC.

Product NDC at billing width43857-0648Add 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
43857-0648-1	43857064801	30 mL in 1 BOTTLE, DROPPER (43857-0648-1)Marketed from Nov 18, 2024

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): Glucoseforce HPSuffix: HP
Generic name (nonproprietary): colchicum autumnale, lacticum acidum, lycopodium clavatum, phosphoricum acidum, phosphorus, syzygium jambolanum, uranium nitricum
Active ingredients: Colchicum autumnale bulb — 30 [hp_X]/mLLactic acid, Dl- — 30 [hp_X]/mLLycopodium clavatum spore — 30 [hp_X]/mLPhosphoric acid — 30 [hp_X]/mLPhosphorus — 30 [hp_X]/mLSyzygium cumini seed — 30 [hp_X]/mLUranyl nitrate hexahydrate — 30 [hp_C]/mL
Dosage form: Liquid
Route: Oral
Labeler: BioActive Nutritional, Inc.
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Nov 18, 2024
Listing expires: Dec 31, 2027
Identifiers: Product ID 43857-0648_02c2483d-58b0-45a5-a221-5383dd06c10dSPL ID 02c2483d-58b0-45a5-a221-5383dd06c10dSPL set ID f1e89586-02ed-4b29-9902-12b17c01bee9UNII 993QHL78E6, 3B8D35Y7S4, C88X29Y479, E4GA8884NN, 27YLU75U4W, 820LSF646I, 3V057702FY

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

N443857064801 followed by a unit qualifier and the quantity

Package 43857-0648-01. 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 Mar 9, 2026.

Indications (excerpt from the label)

USES: For temporary relief of symptoms due to abnormal blood sugar.** **Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)