FDA.reportPublic FDA data

Good Neighbor Roll-on Pain Relief

Manufacturer
Amerisource Bergen | Nantong Health & Beyond Hygienic Products Inc.
Effective date
2025-08-06
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:09:30

Label at a glance#

ProductGood Neighbor Roll-on Pain Relief
Active ingredientLIDOCAINE
Label structure9 sections

Indications and uses

Temporarily relieves minor pain

Dosage and administration

adults and children over 12 years: ■apply a thin layer to affected area every 6 to 8 hours, not to exceed 3 applications in a 24 hour period. children 12 years or younger: ■ask a doctor

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Lidocaine HCL 4%

Purpose

OTC - PURPOSE SECTION

Topical anesthetic

Uses

INDICATIONS & USAGE SECTION

Temporarily relieves minor pain

Warnings

WARNINGS SECTION

For external use only

Do not use

OTC - DO NOT USE SECTION

On large areas of the body or on cut, irritated or swollen skin
■ on puncture wounds

■for more than one week without consulting a doctor

When using this product

OTC - WHEN USING SECTION

■use only as directed. Read and follow all directions and warnings on this carton

■do not allow contact with the eyes and mucous membranes

■ do not bandage or apply local heat (such as heating pads) or a medicated patch to area of use

■do not use at the same time as other topical analgesics

Stop use and ask a doctor if

OTC - STOP USE SECTION

■ condition worsens ■ redness is present
■irritation develops

■symptoms persist for more than 7 days or clear up and occur again within a few days

If pregnant or breastfeeding

OTC - PREGNANCY OR BREAST FEEDING SECTION

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 Poison Control Center (1-800-222-1222) right away.

Directions

DOSAGE & ADMINISTRATION SECTION


adults and children over 12 years:■apply a thin layer to affected area every 6 to 8 hours, not to exceed 3 applications in a 24 hour period.


children 12 years or younger:■ask a doctor

Other information

OTHER SAFETY INFORMATION

Store at room temperature

Inactive Ingredients

INACTIVE INGREDIENT SECTION


acrylates/C10-30 alkyl acrylate crosspolymer (60000 MPA.S), aloe barbadensis leaf juice, am nomethylpropanol, ceteth-10 phosphate, cetostearyl alcohol, cyclomethicone 5, dicetyl phosphate, dimethicone 350, dimethicone/vinyl dimethicone crosspolymer (soft particle),
disodium EDTA, ethylhexylglycerin, glyceryl 1 stearate, hydroxyethyl acrylate/sodium acryloyld methyl taurate copolymer (100000 MPA.S at 1.5%), sohexadecane, phenoxyethanol, SD alcohol, steareth-21, water

Questions or Comments

OTC - QUESTIONS SECTION

Call 1-866-326-1313

Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

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
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
46122-802-29Good Neighbor Roll-on Pain Relief1 in 1 PACKAGELIQUID11
46122-802-29Good Neighbor Roll-on Pain Relief74 mL in 1 BOTTLE, WITH APPLICATORLIQUID741

Products#

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

DailyMed product names page 1 of 1 · 21 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
46122-80246122-802-29

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 19 matching rows.

Name, UNII, Kind table
NameUNIIKind
DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (SOFT PARTICLE)9E4CO0W6C5IACT
EDETATE DISODIUM ANHYDROUS8NLQ36F6MMIACT
ACRYLATES/C10-30 ALKYL ACRYLATE CROSSPOLYMER (60000 MPA.S)8Z5ZAL5H3VIACT
GLYCERYL 1-STEARATE258491E1RZIACT
DIMETHICONE 3502Y53S6ATLUIACT
ETHYLHEXYLGLYCERIN147D247K3PIACT
PHENOXYETHANOLHIE492ZZ3TIACT
ALCOHOL3K9958V90MIACT
ALOE VERA LEAFZY81Z83H0XIACT
STEARETH-2153J3F32P58IACT
ISOHEXADECANE918X1OUF1EIACT
HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER (45000 MPA.S AT 1%)86FQE96TZ4IACT
CYCLOMETHICONE 50THT5PCI0RIACT
CETOSTEARYL ALCOHOL2DMT128M1SIACT
AMINOMETHYLPROPANOLLU49E6626QIACT
DIHEXADECYL PHOSPHATE2V6E5WN99NIACT
CETETH-10 PHOSPHATE4E05O5N49GIACT
WATER059QF0KO0RIACT
LIDOCAINE98PI200987ACTIB

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
Good Neighbor Roll-on Pain ReliefLIDOCAINE HCLAmerisource Bergena0c3adbf-fa35-47c0-9db3-459ce9a106ac2025-08-06WarningsExact identifier
ndc (package): 46122-802-29
ndc (product): 46122-802
ndc11 (package): 46122080229
spl id: 3bb569fe-2142-3bf5-e063-6394a90ab8e4
spl set id: a0c3adbf-fa35-47c0-9db3-459ce9a106ac

Reported adverse events (FAERS/openFDA)#

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