Acetylcholine Chloride NDC 43857-0138

NDC codes

FDA NDC Directory

Product NDC (as listed)43857-0138Labeler and product segments. Claims need a package NDC.

Product NDC at billing width43857-0138Add 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
43857-0138-1	43857013801	30 mL in 1 BOTTLE, DROPPER (43857-0138-1)Marketed from Nov 10, 2016

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): Acetylcholine Chloride
Generic name (nonproprietary): acetylcholine chloride
Active ingredients: Acetylcholine chloride — 6 [hp_X]/mL
Dosage form: Liquid
Route: Oral
Labeler: BioActive Nutritional, Inc.
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Feb 28, 2013
Listing expires: Dec 31, 2026
Other FDA classes: Cholinergic Agonists (Mechanism)
Identifiers: Product ID 43857-0138_88b92968-2286-444b-a39c-c7ac8492e821SPL ID 88b92968-2286-444b-a39c-c7ac8492e821SPL set ID c98abc4d-8539-42e9-954a-5a850f28c9edUNII AF73293C2R
Pharmacologic class: Cholinergic Receptor 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

N443857013801 followed by a unit qualifier and the quantity

Package 43857-0138-01. 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 Nov 10, 2016.

Indications (excerpt from the label)

INDICATIONS: For temporary relief of chest congestion with mild constriction, indigestion, drowsiness, headache, forgetfulness, and general fatigue.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)