What is NDC 17089-372?

17089-372 is the product NDC for Guna-Egf (epidermal growth factor), Human epidermal growth factor 4 [hp_C]/30mL solution/ drops, listed with the FDA by Guna spa. It has 1 package NDC, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

Guna-Egf (Epidermal growth factor).

Guna spa, NDC labeler code 17089. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Guna-Egf?

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.

Guna-Egf NDC 17089-372 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)17089-372Labeler and product segments. Claims need a package NDC.

Product NDC at billing width17089-0372Add 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
17089-372-18	17089037218	1 BOTTLE, DROPPER in 1 BOX (17089-372-18) / 30 mL in 1 BOTTLE, DROPPERMarketed from Mar 31, 2011

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): Guna-Egf
Generic name (nonproprietary): epidermal growth factor
Active ingredients: Human epidermal growth factor — 4 [hp_C]/30mL
Dosage form: Solution/ drops
Route: Oral
Labeler: Guna spaNDC labeler code 17089
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Mar 31, 2011
Listing expires: Dec 31, 2026
Identifiers: Product ID 17089-372_82de46fa-983c-fade-e053-2991aa0aea95SPL ID 82de46fa-983c-fade-e053-2991aa0aea95SPL set ID 6473bd71-5baf-4c42-ac0b-2cfaf69bfd8cUNII TZK30RF92WUPC 0317089372189

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

N417089037218 followed by a unit qualifier and the quantity

Package 17089-0372-18. 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 Dec 21, 2018.

Indications (excerpt from the label)

INDICATIONS & USAGE DIRECTIONS: TAKE 15 MINUTES BEFORE MEALS

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 17089-372

What is NDC 17089-372?: 17089-372 is the product NDC for Guna-Egf (epidermal growth factor), Human epidermal growth factor 4 [hp_C]/30mL solution/ drops, listed with the FDA by Guna spa. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Guna-Egf (Epidermal growth factor).
What is the active ingredient?: Human epidermal growth factor.
Who is the labeler?: Guna spa, NDC labeler code 17089. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Guna-Egf?: 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.

Guna-Egf (Epidermal growth factor) NDC 17089-372