What is NDC 83389-112?

83389-112 is the product NDC for Pro Numb Sensitive Skin (numbing spray), Epinephrine hydrochloride .1 mg/100mL; Lidocaine hydrochloride 4.2 mg/100mL spray, listed with the FDA by Pro Numb Tattoo Numbing Spray LLC. It has 1 package NDC, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

Pro Numb Sensitive Skin (Numbing Spray).

What is the active ingredient?

Epinephrine hydrochloride, Lidocaine hydrochloride.

Pro Numb Tattoo Numbing Spray LLC, NDC labeler code 83389. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Pro Numb Sensitive Skin?

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.

Pro Numb Sensitive Skin NDC 83389-112 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)83389-112Labeler and product segments. Claims need a package NDC.

Product NDC at billing width83389-0112Add 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
83389-112-11	83389011211	120 mL in 1 BOTTLE, SPRAY (83389-112-11)Marketed from Feb 2, 2026

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): Pro Numb Sensitive Skin
Generic name (nonproprietary): numbing spray
Active ingredients: Epinephrine hydrochloride — .1 mg/100mLLidocaine hydrochloride — 4.2 mg/100mL
Dosage form: Spray
Route: Topical
Labeler: Pro Numb Tattoo Numbing Spray LLCNDC labeler code 83389
Product type: Over-the-counter drug
Marketing category: Unapproved drug (other)
Marketing start: Feb 2, 2026
Listing expires: Dec 31, 2027
Other FDA classes: Adrenergic alpha-Agonists (Mechanism)Adrenergic beta-Agonists (Mechanism)Amides (Chemical structure)Catecholamines (Chemical structure)Local Anesthesia (Physiologic effect)
Identifiers: Product ID 83389-112_49de3bed-0ed6-a9f5-e063-6394a90ae7cbSPL ID 49de3bed-0ed6-a9f5-e063-6394a90ae7cbSPL set ID 49de3bf2-f54e-a9a3-e063-6394a90acdcbUNII WBB047OO38, V13007Z41A
Pharmacologic class: Amide Local Anesthetic; Antiarrhythmic; Catecholamine; alpha-Adrenergic Agonist; beta-Adrenergic 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. Topical products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N483389011211 followed by a unit qualifier and the quantity

Package 83389-0112-11. 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 Feb 2, 2026.

Indications (excerpt from the label)

Use Temporarily takes away pain, itching, and swelling associated with anorectal disorders or pain-sensitive procedures.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 83389-112

What is NDC 83389-112?: 83389-112 is the product NDC for Pro Numb Sensitive Skin (numbing spray), Epinephrine hydrochloride .1 mg/100mL; Lidocaine hydrochloride 4.2 mg/100mL spray, listed with the FDA by Pro Numb Tattoo Numbing Spray LLC. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Pro Numb Sensitive Skin (Numbing Spray).
What is the active ingredient?: Epinephrine hydrochloride, Lidocaine hydrochloride.
Who is the labeler?: Pro Numb Tattoo Numbing Spray LLC, NDC labeler code 83389. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Pro Numb Sensitive Skin?: 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.

Pro Numb Sensitive Skin (Numbing spray) NDC 83389-112