Aemerry Numbing Cream

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: Aemerry Numbing Cream
Generic name: MENTHOL 5%
Manufacturer: Da Capo Prima LLC
Product type: HUMAN OTC DRUG
SPL set ID: 4fefddaf-19c8-86b4-e063-6294a90abffc
SPL ID: 4fefddaf-19c9-86b4-e063-6294a90abffc
Version: 1
Effective date: 2026-04-20
Source export date: 2026-09-28
Source partition: 8
Source file: https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/ae3816359e336a5de4f44607730a3d12ceb61ffa012a132189ceda22541b38ee/drug-label-0008-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:56:52

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		M017	openfda.application_number
brand name		Aemerry Numbing Cream	openfda.brand_name
generic name		MENTHOL 5%	openfda.generic_name
manufacturer name		Da Capo Prima LLC	openfda.manufacturer_name
ndc	package	87615-002-01	openfda.package_ndc
ndc	product	87615-002	openfda.product_ndc
ndc11	package	87615000201	derived:openfda.package_ndc
rxcui		1039690	openfda.rxcui
spl id		4fefddaf-19c9-86b4-e063-6294a90abffc	id
spl set id		4fefddaf-19c8-86b4-e063-6294a90abffc	set_id
unii		L7T10EIP3A	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

For external use only Do not use this product if youare allergic to lidocaine. in case of accidental overdose, seek immedidate medical help or contact the Poison Control Center. seal is broken or missing. When using this product donot exceed the recommended daily dosage unless directed by a doctor. Certain sensitive individualsmayhave an allergic reaction to some of the ingredients of this product. do not put this cream into the rectum using your fingers, applicators, or any medical devices. Stop use and ask a doctor if the symptom being treated does not improve, or ifredness,irritation, swelling, pain, or other symptoms appear or worsen. Seek medical help right away. In case of accidental ingestion, seek medical help right away.

Reported adverse events (FAERS/openFDA)#

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