WAXUP Numbing

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: WAXUP Numbing
Generic name: LIDOCAINE HYDROCHLORIDE
Manufacturer: CONSTRUSOLUTION, LLC
Product type: HUMAN OTC DRUG
SPL set ID: 4f1645ab-1b19-4d69-99c3-9ea275b01a87
SPL ID: 0976ef49-eccc-1b67-e063-6294a90a4ec6
Version: 2
Effective date: 2023-11-06
Source export date: 2026-09-28
Source partition: 12
Source file: https://download.open.fda.gov/drug/label/drug-label-0012-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/663999d0fe1757c1e2cd13a4799d76d875f663e0bc57701092264ebe7febfc18/drug-label-0012-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 06:24:09

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 · 11 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M015	openfda.application_number
brand name		WAXUP Numbing	openfda.brand_name
generic name		LIDOCAINE HYDROCHLORIDE	openfda.generic_name
manufacturer name		CONSTRUSOLUTION, LLC	openfda.manufacturer_name
ndc	package	83163-386-00	openfda.package_ndc
ndc	product	83163-386	openfda.product_ndc
ndc11	package	83163038600	derived:openfda.package_ndc
rxcui		2624687	openfda.rxcui
spl id		0976ef49-eccc-1b67-e063-6294a90a4ec6	id
spl set id		4f1645ab-1b19-4d69-99c3-9ea275b01a87	set_id
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: For external use only. Do not: exceed the recommended daily dosage unless directed by a doctor. put this product into the rectum by using fingers or any mechanical device or applicator. When using this product: If condition worsens or does not improve within 7 days, consult a doctor. In case of bleeding, consult a doctor promptly. Stop use and ask a doctor if: If the symptom being treated does not subside or if redness, irritation, swelling, pain, or other symptoms develop or increase. Certain persons can develop allergic reactions to ingredients in this product. Allergy alert: Keep out of raech of children. If swallowed, get medical help, or contact a Poison Control Center right away. If pregnant or breast-feeding, ask a health professional before use.

Reported adverse events (FAERS/openFDA)#

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