Pro Numb
Tattoo Numbing Spray · Spray · Topical
Active ingredient
Active Ingredient(s) Lidocaine HCI 5% Epinephrine HCI .01%
Purpose
Purpose Topical Anesthetic
Uses
Use Temporarily takes away pain, itching, and swelling associated with anorectal disorders or pain-sensitive procedures.
Warnings
Warnings External Use Only. Keep out of reach of children. Do not use if you have
• seizures or liver disease
• if pregnant or breastfeeding
• a known allergy or sensitivity occurs, discontinue use, and seek medical attention. If the condition intensifies or symptoms persist for more than seven days or clear up and occur again within a few days, Cease the use of this product and consult a doctor. Do not use in large quantities, Particularly over raw surfaces or blistered areas. Avoid contact with the eyes. If contact should occur, irrigate with large amounts of sterile saline and seek medical attention. Do not swallow, if swallowed, seek medical attention immediately. When using this product, you may notice temporary whiting or redness of the skin where pro numb is applied.
Keep out of reach of children
Keep out of reach of children.
Directions
Directions A sensitivity test is encouraged before using. Spray a small amount on the broken area of the skin. Wait 60 seconds for the anesthetic to start working. Wash Pro Numb off completely before tattooing.
Other information
Other information Store in a cool dark place or refrigerate and keep out of reach of children. Discard the item after the expiration date is due.
Inactive ingredients
Inactive ingredients purified RO water, Paraben-DU, Disodium EDTA, Citric acid, Optiphen.
Questions?
Call: (800) 865-4965
Label text from the FDA structured product label by Pro Numb Tattoo Numbing Spray LLC (revised Dec 5, 2025). Long sections are shortened; the complete label is on DailyMed.
Active ingredients
- Epinephrine Hydrochloride in 1 product
- Lidocaine Hydrochloride in 1 product
Pro Numb NDC products (1)
| NDC | Strength & form | Labeler | Type |
|---|---|---|---|
| 83389-111 | Epinephrine Hydrochloride .1 mg/100mL; Lidocaine Hydrochloride 5 mg/100mL Spray | Pro Numb Tattoo Numbing Spray LLC | UNAPPROVED DRUG OTHER |
Pro Numb recalls
- D-0302-2026 Feb 18, 2026 · Class II · Ongoing
cGMP deviations
Frequently asked questions
What is Pro Numb used for?
Use Temporarily takes away pain, itching, and swelling associated with anorectal disorders or pain-sensitive procedures.
Who makes Pro Numb?
Pro Numb is listed by 1 labeler in the FDA NDC directory, including Pro Numb Tattoo Numbing Spray LLC.
Has Pro Numb been recalled?
The FDA enforcement database lists 1 recall for Pro Numb, most recently D-0302-2026 (class ii): cGMP deviations