GC 163 Lidocaine Pain Relief Patch

Manufacturer
GERI-CARE PHARMACEUTICAL CORP
Effective date
2026-05-13
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:58:08

Label at a glance#

ProductLidocaine Pain Relief Patch
Active ingredientLIDOCAINE
Label structure11 sections

Dosage and administration

Adults and children 12 years of age and over: Clean and dry affected area. Carefully remove backing from patch (see illustration). Apply sticky side of patch to affected area. Use one patch for up to 12 hours. Discard patch after single use. Children under 12 years of age: consult a physician.

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Lidocaine 4.0%

Purpose

OTC - PURPOSE SECTION

Topical Anesthetic

Use

INDICATIONS & USAGE SECTION

Temporaily relieves minor pain.

Warnings

WARNINGS SECTION

For external use only.

Do not us​e ■ More than one patch on your body at a time ■ On cut, irritated or swollen skin
■ On puncture wounds ■ For more than one week without consulting a doctor
■ If you are allergic to any active or inactive ingredients
When using this product ■ Use only as directed
■ Read and follow all directions and warnings on this carton ■ Do not allow contact with the eyes
■ Do not use at the same time as other topical analgesics ■ Do not microwave
■ Do not bandage tightly or apply local heat (such as heating pads) to the area of use
■ Dispose of used patch in manner that always keeps product away from children and pets. Used
patches still contain the drug product that can produce serious adverse effects if a child or pet
chews or ingests this patch.
Stop use and consult a doctor if ■ Condition worsens ■ Redness is present ■ Irritation develops
■ Symptoms persist for more than 7 days or clear up and occur again within a few days ■ You
experience signs of skin injury, such as pain, swelling or blistering where the product was applied.

OTC - PREGNANCY OR BREAST FEEDING SECTION

If pregnant or breastfeeding, ask a health professional before use.

Keep out of reach of children and pets.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) right away.

Directions

DOSAGE & ADMINISTRATION SECTION

Adults and children 12 years of age and over: Clean and dry affected area. Carefully remove
backing from patch (see illustration). Apply sticky side of patch to affected area. Use one patch
for up to 12 hours. Discard patch after single use.
Children under 12 years of age: consult a physician.

Other Information

OTHER SAFETY INFORMATION

■ Store at room temperature ■ Avoid direct sunlight ■ Protect from excessive moisture

Inactive Ingredients

INACTIVE INGREDIENT SECTION

aluminum glycinate, benzyl alcohol, butylated hydroxyanisole, carboxymethylcellulose sodium,
edetate disodium, ethylhexylglycerin, glycerin, kaolin, methacrylate copolymer, oleic acid,
phenoxyethanol, polyacrylic acid, polysorbate 80, polyvinyl alcohol, propylene glycol, PVP, sodium
polyacrylate, sorbitol, tartaric acid, titanium dioxide, water

Questions or comments:

OTC - QUESTIONS SECTION

Call 1-800-540-3765

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

11

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1737778lidocaine 4 % Medicated PatchPSN1
1737778lidocaine 0.04 MG/MG Medicated PatchSCD1
1737778lidocaine 4 % Medicated PatchSY1

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
LIDOCAINE Pharmacologic Class Indexing2Indexing - Pharmacologic Class20180813

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
070fbed5-7088-434a-a7ce-f2a64d8d40acProduct name220260107
bee66ce1-adb7-9d3b-67d9-582e4c54e80fProduct name520250819
860a93dc-4863-49cc-b284-6bbe8191bc48Product name420250214
eaba870a-6a9d-442e-8643-87b3f558a451Product name120250117
9b4cf230-fd05-41d5-98c6-5db9ecb27b86Product name120230117
7d755fa1-1087-4dcd-98f0-6d4bba479a57Product name320210602
f52be47f-7aa7-46c0-b1fa-50c18dd50206Product name120201029
aed701d5-9c75-dfaf-7154-cde46179faeaProduct name920200313
fa8b5901-e681-426f-82fe-54f6d81ec698Product name420180619
332d03e4-aa24-4b11-841a-02bf41081920Product name120171221
c08ab52f-2fc8-4409-9d9f-ed8edc0bd070Product name120171221
68ed98f8-24c2-44a0-944a-6d36e82ce25aProduct name120141222
1cd42bc2-a430-c72b-636d-991b235fbf80Product name120140508
49fa150c-f0de-cce7-3d9c-993ed81c5698Product name120140508
4d7ae718-ed00-bae8-2abe-9eaec1eef7ffProduct name120140508
9137811f-f279-8640-5aeb-99fa2145d64dProduct name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
57896-163-01Lidocaine Pain Relief Patch350 mg in 1 PATCHPATCH3501
57896-163-05Lidocaine Pain Relief Patch5 in 1 CARTONPATCH51

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
57896-163-05EA - Each57896-1632f3c9a29-8c9d-4415-a212-c7de8a4f50d312026-05-22

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 23 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
57896-16357896-163-01, 57896-163-05

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 22 matching rows.

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Lidocaine Pain Relief PatchLIDOCAINEGERI-CARE PHARMACEUTICAL CORP51b7753b-8619-6ea9-e063-6294a90a4ea42026-05-13WarningsExact identifier
ndc (package): 57896-163-01
ndc (package): 57896-163-05
ndc (product): 57896-163
ndc11 (package): 57896016305
ndc11 (package): 57896016301
spl id: 51b76a76-b449-18fe-e063-6294a90af613
spl set id: 51b7753b-8619-6ea9-e063-6294a90a4ea4

Reported adverse events (FAERS/openFDA)#

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