What is NDC 41250-495?

41250-495 is the product NDC for Meijer Anti Nausea, Dextrose, Unspecified form 1.87 g/5mL + 2 more ingredients liquid, listed with the FDA by MEIJER DISTRIBUTION, INC.. It has 1 package NDC, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

Meijer Anti Nausea (Dextrose(glucose),Levulose(fructose),Phosphoric acid).

What is the active ingredient?

Dextrose, Unspecified form, Fructose, Phosphoric acid.

MEIJER DISTRIBUTION, INC., NDC labeler code 41250. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Meijer Anti Nausea?

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.

Meijer Anti Nausea NDC 41250-495 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)41250-495Labeler and product segments. Claims need a package NDC.

Product NDC at billing width41250-0495Add 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
41250-495-04	4125004950441250049504	1 BOTTLE in 1 CARTON (41250-495-04) / 118 mL in 1 BOTTLEMarketed from Jun 29, 2020

How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 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): Meijer Anti Nausea
Generic name (nonproprietary): dextrose(glucose),levulose(fructose),phosphoric acid
Active ingredients: Dextrose, Unspecified form — 1.87 g/5mLFructose — 1.87 g/5mLPhosphoric acid — 21.5 mg/5mL
Dosage form: Liquid
Route: Oral
Labeler: MEIJER DISTRIBUTION, INC.NDC labeler code 41250
Product type: Over-the-counter drug
Marketing category: Unapproved drug (other)
Marketing start: Jun 29, 2020
Listing expires: Dec 31, 2027
Identifiers: Product ID 41250-495_bfca0350-6ddd-43e0-98ce-e1d5b9a53a07SPL ID bfca0350-6ddd-43e0-98ce-e1d5b9a53a07

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

N441250049504 followed by a unit qualifier and the quantity

Package 41250-0495-04. 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

The FDA listing for this product does not reference a label (SPL) set.

About NDC 41250-495

What is NDC 41250-495?: 41250-495 is the product NDC for Meijer Anti Nausea, Dextrose, Unspecified form 1.87 g/5mL + 2 more ingredients liquid, listed with the FDA by MEIJER DISTRIBUTION, INC.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Meijer Anti Nausea (Dextrose(glucose),Levulose(fructose),Phosphoric acid).
What is the active ingredient?: Dextrose, Unspecified form, Fructose, Phosphoric acid.
Who is the labeler?: MEIJER DISTRIBUTION, INC., NDC labeler code 41250. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Meijer Anti Nausea?: 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.