MEB Gluco-Vitality Patch

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: MEB Gluco-Vitality Patch
Generic name: MEB GLUCO-VITALITY PATCH
Manufacturer: Kadesh Incoporation Co,Ltd
Product type: HUMAN OTC DRUG
SPL set ID: 00daa9e5-c82a-c272-e063-6294a90ab5a9
SPL ID: 0339df62-44db-fd6e-e063-6394a90aa997
Version: 3
Effective date: 2023-08-18
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 05:19:55

Harmonized routes table
Harmonized routes
TRANSDERMAL

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 · 27 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
brand name		MEB PainGuard Patch	openfda.brand_name
brand name		MEB Gluco-Vitality Patch	openfda.brand_name
generic name		MEB PAINGUARD PATCH	openfda.generic_name
generic name		MEB GLUCO-VITALITY PATCH	openfda.generic_name
manufacturer name		Kadesh Incoporation Co,Ltd	openfda.manufacturer_name
ndc	package	81488-011-30	openfda.package_ndc
ndc	package	81488-010-30	openfda.package_ndc
ndc	product	81488-010	openfda.product_ndc
ndc	product	81488-011	openfda.product_ndc
ndc11	package	81488001030	derived:openfda.package_ndc
ndc11	package	81488001130	derived:openfda.package_ndc
spl id		0339df62-44db-fd6e-e063-6394a90aa997	id
spl set id		00daa9e5-c82a-c272-e063-6294a90ab5a9	set_id
unii		27YLU75U4W	openfda.unii
unii		02F3473H9O	openfda.unii
unii		O3B55K4YKI	openfda.unii
unii		42Z2K6ZL8P	openfda.unii
unii		0I2XIN602U	openfda.unii
unii		91GQH8I5F7	openfda.unii
unii		8M4L3H2ZVZ	openfda.unii
unii		SK47B8698T	openfda.unii
unii		24H4NWX5CO	openfda.unii
unii		70FD1KFU70	openfda.unii
unii		00J9J9XKDE	openfda.unii
unii		E1UOL152H7	openfda.unii
unii		S4255P4G5M	openfda.unii
unii		J41CSQ7QDS	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

Do not Use *If the needles inside the patch do not cause a tingling sensation, do not use it and replace it with a new patch. *If headaches, dizziness, or any discomfort persist for more than 5 minutes, discontinue use. Consult a physician if: *Symptoms persist for more than 7 days or worsen. When using this product: *Due to its sensitivity to moisture, do not store the patch in the refrigerator, and it should be used immediately after opening. Keep out of reach of Children

Reported adverse events (FAERS/openFDA)#

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