Meijer Pain Lidocaine Plus Relieving

Manufacturer
Meijer Distribution, Inc | Garcoa, Inc. | SV Labs Toronto Corporation
Effective date
2024-11-15
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
monthly-update
Hydrated at
2026-06-03 17:51:55

Label at a glance#

ProductMeijer Pain Lidocaine Plus Relieving Analgesic
Active ingredientBENZYL ALCOHOL, LIDOCAINE HYDROCHLORIDE
Label structure10 sections

Dosage and administration

Adults and children 12 years age and older clean and dry affected area apply to affected area not more than 3 to 4 times daily. Children under 12 years of age: consult a doctor.

Storage and handling

protect the product in the container from excessive heat, moisture or direct sun store with lid closed tightly.

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

OTC - ACTIVE INGREDIENT SECTION

OTC - PURPOSE SECTION

Active ingredients Purpose
Benzyl Alcohol (10%)Topical analgesic
Lidocaine (HCl 4%)Topical analgesic

Use

INDICATIONS & USAGE SECTION

for the temporary relief of pain

Warnings

WARNINGS SECTION

SPL UNCLASSIFIED SECTION

For external use only

Flammable

SPL UNCLASSIFIED SECTION

Keep away from fire or flame

Do not use

OTC - DO NOT USE SECTION

If you ever had an allergic reaction to this product or any of its ingredients.

When using this product

OTC - WHEN USING SECTION

  • avoid contact with the eyes
  • do not use on damaged or broken skin
  • do not bandage tightly
  • do not use in large quantities, particularly over raw surfaces or blistered areas
  • do not use with heating pads, medicated patches or heating devices
  • use only as directed.

Stop use and ask a doctor if

OTC - STOP USE SECTION

  • condition worsens, or if symptoms persist for more than 7 days or clear up and occur again within a few days
  • pain, swelling, blistering develops where product is used
  • redness, rash, itching, irritation develops where product is used.

OTC - PREGNANCY OR BREAST FEEDING SECTION

If you are pregnant or nursing, seek the advice of a health professional before using.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. 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 age and older

  • clean and dry affected area
  • apply to affected area not more than 3 to 4 times daily. Children under 12 years of age: consult a doctor.

Other information

STORAGE AND HANDLING SECTION

  • protect the product in the container from excessive heat, moisture or direct sun
  • store with lid closed tightly.

Inactive ingredients

INACTIVE INGREDIENT SECTION

alcohol denat., aloe barbadensis leaf juice, aminomethyl propanol, carbomer, water.

Questions or comments?

OTC - QUESTIONS SECTION

1-866-567-8600

SPL UNCLASSIFIED SECTION

DIST. BY MEIJER DISTRIBUTION, INC.
GRAND RAPIDS, MI 49544

PRINCIPAL DISPLAY PANEL - 88 mL Cylinder Carton

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

meijer®

Compare to
Salonpas® LIDOCAINE
PLUS Pain Relieving
Liquid Active
Ingredients*

lidocaine plus
pain relieving
liquid

Benzyl alcogol 10%
Lidocaine 4%

No-Mess Applicator

TOPICAL ANALGESIC

Helps to numb
away pain

Fragrance free,
non-greasy, fast
acting formula

3 FL OZ (88 mL)

Principal Display Panel - 88 mL Cylinder Carton
Principal Display Panel - 88 mL Cylinder Carton

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1943537benzyl alcohol 10 % / lidocaine HCl 4 % Topical SolutionPSN4
1943537benzyl alcohol 0.1 ML/ML / lidocaine hydrochloride 40 MG/ML Topical SolutionSCD4
1943537benzyl alcohol 10 % / lidocaine HCl 4 % Topical SolutionSY4

DailyMed Pharmacologic Classes#

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

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
860a93dc-4863-49cc-b284-6bbe8191bc48Product name420250214
eaba870a-6a9d-442e-8643-87b3f558a451Product name120250117
9b4cf230-fd05-41d5-98c6-5db9ecb27b86Product name120230117
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

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
79481-0084-1Meijer Pain Lidocaine Plus RelievingAnalgesic1 in 1 CARTONLIQUID14
79481-0084-1Meijer Pain Lidocaine Plus RelievingAnalgesic88 mL in 1 CYLINDERLIQUID884

Products#

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

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
79481-008479481-0084-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
32024-11-15full-release2026-06-01 01:17:55

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
Meijer Pain Lidocaine Plus Relieving AnalgesicBENZYL ALCOHOL AND LIDOCAINE HYDROCHLORIDEMeijer Distribution, Incb7385140-3f63-4cbc-b557-de1d29d1ea362024-11-15WarningsExact identifier
ndc (package): 79481-0084-1
ndc (product): 79481-0084
ndc11 (package): 79481008401
spl id: 115871ae-4a0c-4e20-9103-8327635ee318
spl set id: b7385140-3f63-4cbc-b557-de1d29d1ea36

Reported adverse events (FAERS/openFDA)#

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