Class II · Moderate risk
Pro Numb Tattoo Numbing Spray
cGMP deviations
National Drug Code
Is NDC 83389-0112-11 recalled?
Pro Numb Sensitive Skin · 120 mL in 1 BOTTLE, SPRAY (83389-112-11)
Yes — this exact package was recalled
1 FDA recall names the code 83389-0112-11 directly. A recall still applies to particular lot numbers — compare the lot on your package with the FDA notice below, and talk to your pharmacist before stopping a prescribed medication.
1 of these recalls is still ongoing.
- Active ingredient
- Numbing Spray
- Strength
- EPINEPHRINE HYDROCHLORIDE .1 mg/100mL; LIDOCAINE…
- Form
- Spray · Topical
- Labeler
- Pro Numb Tattoo Numbing Spray LLC
- Type
- Human OTC Drug
- Product code
- 83389-0112
Recalls naming this package
Where to find this code. The NDC is printed on the pharmacy label and on the manufacturer's carton, usually as three groups of digits after “NDC”. The last group is the package size — two bottles of the same medicine can differ only in that group, and a recall may cover one but not the other.
Other recalled products from this labeler
- 83389-0111 Pro Numb 1
Free recall alerts
Know the day your medication is recalled
Tell us what you take. When FDA posts a recall announcement or classifies a recall for one of your medications, we email you in plain English, with what to check. No account needed.