pain relief cream

Manufacturer
AEC Consumer Products | Cospro Development Corp
Effective date
2021-01-05
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:36:29

Label at a glance#

Productpain relief cream
Active ingredientLIDOCAINE HYDROCHLORIDE
Label structure14 sections

Dosage and administration

Adults and children over 12 years: apply as needed to affected areas 3-4 times a day. Consult a physician if pain persists. 

Storage and handling

Apply as needed to affectedareas 3-4 times a day.

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient                                                                                        Purpose
Lidocaine Hydrochloride 4%.......................................................................External Analgesic

Purpose

OTC - PURPOSE SECTION

External Analgesic

Warning

WARNINGS SECTION

For External use only

When using this product

OTC - WHEN USING SECTION

When using this product use only as directed

  • avoid contact with the eyes
  • do not bandage or apply local heat (such as heating pads) to the area of use

Stop use and ask a doctor if

OTC - STOP USE SECTION

Stop use and ask a doctor if condition worsens symptoms persist more than 7 days

symptoms clear up and occur again with a few days

Keep out of use of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of use of children. If swallowed, get medical help or contact a Poison Control Center right away

Storage and Handling

STORAGE AND HANDLING SECTION

Apply as needed to affectedareas 3-4 times a day.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Allantoin, Aqua, Arnica Mountain Flower Extract, Astaxanthin, Benzyl Alcohol, BHT, Bisabolol, Boswellia Serrata Resin Extract, Cannabis Sativa Oil/Extract, Cetyl Alcohol, Citrus Aurantium Bergamia Peel Oil, Curcurria Longa Root Extract, Cyclopentasiloxane, Dimethicone, Dimethicol, Emu Oil, Ethoxydiglycol, Glucosamine, Glycerin, Glyceryl Stearate SE, Isopropyl Palmitate, Melaleuca Alternifolia Leaf Oil, Methylsulfonylmethane, PEG-100 Stearate, Phenoxyethanol, Polyquaterium-10, Potassium Sorbate, Propylene Glycol, Retinyl Palmitate, Salicylic Acid, Sodium Hydroxide, Stearic Acid, Stearyl Alcohol, Tetrasodium EDTA, Tocopherol, Triethanolamine, Vaccinium Myrtillus Fruit/Leaf Extract

Indications

INDICATIONS & USAGE SECTION

Use

For the temporary relief of pain

Do not use

OTC - DO NOT USE SECTION

Do not use in large quantities, particularly over raw or blistered surfaces for more than one week without consulting a doctor

Ask a doctor

OTC - ASK DOCTOR SECTION

Ask a doctor if condition worsens symptoms persist more than 7 days symptoms clear up and occur again with a few days

Directions

INSTRUCTIONS FOR USE SECTION

Adults and children over 12 years: apply as needed to affected areas 3-4 times a day. Consult a physician if pain persists. 

dosage

DOSAGE & ADMINISTRATION SECTION

Apply as needed to affected areas 3-4 times a day.

image of label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image of labelimage of label

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
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

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
86089-222-012022-07-29C16284748780-1e4f33bdf-9f2a-d8a0-e053-dadaa90a6e4eDrug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
86089-222-01pain relief cream94.6 g in 1 TUBECREAM94.62

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
86089-222PAIN RELIEF CREAM (LIDOCREAM HYDROCHLORIDE) CREAM [AEC CONSUMER PRODUCTS]2Legacy NDC, 1 package rows20210106_fe1d98da-59eb-4742-94ff-8431ea601f0c.zip

Products#

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

DailyMed product names page 1 of 1 · 33 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
86089-22286089-222-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 29 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
0833f413-d338-48b9-af6b-7c4c70dc4a91fe1d98da-59eb-4742-94ff-8431ea601f0c2021-01-05WarningsExact identifier
spl id: 0833f413-d338-48b9-af6b-7c4c70dc4a91
spl set id: fe1d98da-59eb-4742-94ff-8431ea601f0c

Reported adverse events (FAERS/openFDA)#

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