Swiftalyn 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: Swiftalyn Numbing Cream
Generic name: MENTHOL 1%
Manufacturer: GENUINE INNOVATION LTD
Product type: HUMAN OTC DRUG
SPL set ID: 4b2ebff2-2f50-e54b-e063-6294a90aaccb
SPL ID: 4b2ebff2-2f51-e54b-e063-6294a90aaccb
Version: 1
Effective date: 2026-02-19
Source export date: 2026-09-28
Source partition: 3
Source file: https://download.open.fda.gov/drug/label/drug-label-0003-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/fd09911bd1bc81f7f2faeb048e63855fe224e494376ae919a0035190e315c050/drug-label-0003-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:20:20

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
application number		M017	openfda.application_number
brand name		Swiftalyn Numbing Cream	openfda.brand_name
generic name		MENTHOL 1%	openfda.generic_name
manufacturer name		GENUINE INNOVATION LTD	openfda.manufacturer_name
ndc	package	87013-003-01	openfda.package_ndc
ndc	product	87013-003	openfda.product_ndc
ndc11	package	87013000301	derived:openfda.package_ndc
spl id		4b2ebff2-2f51-e54b-e063-6294a90aaccb	id
spl set id		4b2ebff2-2f50-e54b-e063-6294a90aaccb	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 ■ avoid contact with eyes or mucous membranes ■ Use only as directed ■ condition worsens or does not improve within 7 days ■ allergic reaction occurs to ingredients in this product ■ symptoms being treated do not subside or if redness, irritation, swelling, pain, or other symptoms develop or increase If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) right away.

Reported adverse events (FAERS/openFDA)#

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