Walgreens

Primary DI
00182097000412
Brand
Walgreens
Company
WALGREEN CO.
Model
Bite Relief
Device description
Piezo-electric stimulator for temporary reduction of itching and swelling resulting from mosquito bites
Published
2018-12-21
Public version status
New
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
false
OTC
true
Sterile
false
Single use
false

Contact Domains#

Product Codes#

Code, Name table
CodeName
OSGPiezo-Electric Stimulator For Relief Of Mosquito Bite Itch

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
OSGPiezo-Electric Stimulator For Relief Of Mosquito Bite ItchNeurology2

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
00182097000412Direct MarkingGS10
10311917206728PackageGS1384In Commercial Distribution
20311917206725PackageGS18In Commercial Distribution
00311917206721PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
00182097000412001820970004121820970004120182097000412
1031191720672810311917206728
2031191720672520311917206725
00311917206721003119172067213119172067210311917206721

GMDN Terms#

Term, Definition table
TermDefinition
Insect bite/sting electrical stimulatorA portable, manual device intended to be used for the external treatment of insect bites or stings (e.g., from mosquitoes) through dispatch of a small (e.g., 13 kV) piezeoelectric charge to the affected region of the skin. The charge is intended to localize the poison and inhibit histamine release therefore reducing itching and inflammation. It typically consists of a pocket-sized, hand-held housing containing piezocrystal with a trigger mechanism. It is available [non-prescription] over-the-counter (OTC) for home-use. This is a reusable device.

Sterilization Methods#

Method table
Method

Contacts#

Phone, Email table
PhoneEmail
1-800-925-4733consumerrelations.pq@walgreens.com

Regulatory Flags#

DUNS number
008965063
Device count
1
DM exempt
false
Premarket exempt
false
HCT/P
false
Kit
false
Combination product
false
Lot or batch
true
Serial number
false
Manufacturing date on label
false
Expiration date on label
false
Donation ID number
false
Contains natural rubber latex
false
No natural rubber latex
false
Sterilization required before use
false

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
00311917025360Walgreens6545679288572016-12-20
00311917048154Walgreens6548829288582016-12-20
00311917085685Walgreens7208802026-05-08
00311917085692Walgreens7208932026-05-08
00311917085739Walgreens7208942026-05-08
00311917085753Walgreens7208922026-05-08
00311917085760Walgreens7208972026-05-08
00311917077598Walgreens7377342026-04-28
00311917151434Walgreens2205442019-11-29
00311917151472Walgreens2205502019-11-28
00311917219288Walgreens2729422020-11-26
00311917219295Walgreens2729432020-11-26
00311917064635Walgreens351587 2025-06-20
00311917006239Walgreens2964622023-01-25
00311917065724Walgreens8246332025-04-29
00311917065731Walgreens8246322025-04-29
00311917065762WALGREENS8416972025-04-29
00311917065779WALGREENS7456072025-04-29
00311917066585WALGREENS8360682025-04-29
00311917199603WALGREENS8281472022-03-25

Other Devices Sharing Product Codes#

Primary DI, Brand, Company table
Primary DIBrandCompanyProduct codePublished
00850044118946iHealthiHealth Labs Inc.OSG2026-04-16
00311917206721WalgreensWALGREEN CO.OSG2018-12-21
00182097000368TECNIMEDTECNIMED SRLOSG2018-05-15
00182097000382TECNIMEDTECNIMED SRLOSG2018-05-15
00182097000023TecnibrandsTECNIMED SRLOSG2017-08-02