What is NDC 73519-001?

73519-001 is the product NDC for Babysons (dexpanthenol), Dexpanthenol 50 mg/g ointment, listed with the FDA by Laboratorios Quimica Son's, S.A. de C.V. It has 1 package NDC, shown above in 10- and 11-digit form.

Laboratorios Quimica Son's, S.A. de C.V, NDC labeler code 73519. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Babysons?

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.

Babysons NDC 73519-001 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)73519-001Labeler and product segments. Claims need a package NDC.

Product NDC at billing width73519-0001Add 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
73519-001-30	73519000130	1 TUBE in 1 BOX (73519-001-30) / 30 g in 1 TUBEMarketed from Jun 15, 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): Babysons
Generic name (nonproprietary): dexpanthenol
Active ingredients: Dexpanthenol — 50 mg/g
Dosage form: Ointment
Route: Topical
Labeler: Laboratorios Quimica Son's, S.A. de C.VNDC labeler code 73519
Product type: Over-the-counter drug
Marketing category: Unapproved drug (other)
Marketing start: Jun 15, 2020
Listing expires: Dec 31, 2026
Identifiers: Product ID 73519-001_25cb134c-b31f-af58-e063-6394a90adbb7SPL ID 25cb134c-b31f-af58-e063-6394a90adbb7SPL set ID 8a4782fc-5917-4f63-b9bf-6597be2afc6cRxCUI 249792UNII 1O6C93RI7Z

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. Topical products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N473519000130 followed by a unit qualifier and the quantity

Package 73519-0001-30. 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 Oct 31, 2024.

Indications (excerpt from the label)

Uses Helps treat and prevent diaper rash Protects chafed skin due to diaper rash and helps seal out wetness

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 73519-001

What is NDC 73519-001?: 73519-001 is the product NDC for Babysons (dexpanthenol), Dexpanthenol 50 mg/g ointment, listed with the FDA by Laboratorios Quimica Son's, S.A. de C.V. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Babysons (Dexpanthenol).
What is the active ingredient?: Dexpanthenol.
Who is the labeler?: Laboratorios Quimica Son's, S.A. de C.V, NDC labeler code 73519. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Babysons?: 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.

Babysons (Dexpanthenol) NDC 73519-001