What is NDC 76420-351?

76420-351 is the product NDC for Eha (lidocaine hydrochloride), Lidocaine hydrochloride 4 g/mL lotion, listed with the FDA by Asclemed USA, Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.

Asclemed USA, Inc., NDC labeler code 76420. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Eha?

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.

Eha NDC 76420-351 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)76420-351Labeler and product segments. Claims need a package NDC.

Product NDC at billing width76420-0351Add 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
76420-351-30	76420035130	88 mL in 1 BOTTLE (76420-351-30)Marketed from Jun 7, 2016

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): Eha
Generic name (nonproprietary): lidocaine hydrochloride
Active ingredients: Lidocaine hydrochloride — 4 g/mL
Dosage form: Lotion
Route: Topical
Labeler: Asclemed USA, Inc.NDC labeler code 76420
Product type: Prescription drug
Marketing category: Unapproved drug (other)
Marketing start: Jun 7, 2016
Listing expires: Dec 31, 2026
Other FDA classes: Amides (Chemical structure)Local Anesthesia (Physiologic effect)
Identifiers: Product ID 76420-351_7d77ecf6-5731-d43e-e053-2991aa0af0dbSPL ID 7d77ecf6-5731-d43e-e053-2991aa0af0dbSPL set ID 09835640-55c3-4bfa-9ad3-15d37f06e871UNII V13007Z41AUPC 0376420351306
Pharmacologic class: Amide Local Anesthetic; Antiarrhythmic

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

N476420035130 followed by a unit qualifier and the quantity

Package 76420-0351-30. 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 Nov 1, 2018.

Indications (excerpt from the label)

Uses For temporary relief of pain and itching and minor skin irritations due to minor cuts and scrapes, sunburns, and minor burns.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 76420-351

What is NDC 76420-351?: 76420-351 is the product NDC for Eha (lidocaine hydrochloride), Lidocaine hydrochloride 4 g/mL lotion, listed with the FDA by Asclemed USA, Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Eha (Lidocaine Hydrochloride).
What is the active ingredient?: Lidocaine hydrochloride.
Who is the labeler?: Asclemed USA, Inc., NDC labeler code 76420. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Eha?: 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.

Eha (Lidocaine hydrochloride) NDC 76420-351