Pro Numb

openFDA label record#

This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.

Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)

Brand name: Pro Numb
Generic name: TATTOO NUMBING SPRAY
Manufacturer: Pro Numb Tattoo Numbing Spray LLC
Product type: HUMAN OTC DRUG
SPL set ID: f923860d-977a-c55f-e053-6294a90ae982
SPL ID: 45375094-9ea8-2376-e063-6394a90a57ea
Version: 4
Effective date: 2025-12-05
Source export date: 2026-10-30
Source partition: 6
Source file: https://download.open.fda.gov/drug/label/drug-label-0006-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-30/e37bebe0ee356110e46fe9b102632217cd5fd64caa93a64cf6ef0d92a0bfdb4c/drug-label-0006-of-0014.json.zip
Source manifest SHA-256: b11f1f6b476c7417db937215bf14307ef1a0b69465b42b411ad52f42ae36ead3
Import run: 20261102T182004Z
Imported at: 2026-11-02 18:52:41

Harmonized routes table
Harmonized routes
TOPICAL

Harmonized identifier links#

Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.

Harmonized identifiers page 1 of 1 · 10 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
brand name		Pro Numb	openfda.brand_name
generic name		TATTOO NUMBING SPRAY	openfda.generic_name
manufacturer name		Pro Numb Tattoo Numbing Spray LLC	openfda.manufacturer_name
ndc	package	83389-111-11	openfda.package_ndc
ndc	product	83389-111	openfda.product_ndc
ndc11	package	83389011111	derived:openfda.package_ndc
spl id		45375094-9ea8-2376-e063-6394a90a57ea	id
spl set id		f923860d-977a-c55f-e053-6294a90ae982	set_id
unii		WBB047OO38	openfda.unii
unii		V13007Z41A	openfda.unii

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 1 of 1 · 1 matching rows.

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.

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.