Nervive Pain Relieving

Manufacturer
The Procter & Gamble Manufacturing Company
Effective date
2024-07-30
Label type
HUMAN OTC DRUG LABEL
Version
8
Source
legacy-cache
Hydrated at
2026-08-01 20:57:58

Label at a glance#

ProductNervive Pain Relieving Liquid Roll-on
Active ingredientLIDOCAINE, MENTHOL
Label structure15 sections

Dosage and administration

adults and children over 12 years: • apply a thin layer to affected area every 6 to 8 hours • do not exceed 3 applications in a 24 hour period • massage into painful area until thoroughly absorbed into skin AFTER APPLYING, WASH HANDS WITH SOAP AND WAT ER children 12 years or younger: ask a doctor Store at no greater than 25°C (77°F).

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Lidocaine HCl 4%

Menthol 1%

Active ingredients Purpose

OTC - PURPOSE SECTION

Topical anesthetic

Topical analgesic

Use

INDICATIONS & USAGE SECTION

temporarily relieves minor pain

Warnings

WARNINGS SECTION

For external use only

Flammable •
keep away from heat and open flame

Do not use

OTC - DO NOT USE SECTION

• If you have had an allergic reaction to lidocaine or other local anesthetics

• on large areas of the body or on cut, irritated, blistered, 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.

• avoid contact with eyes and mucous membranes

• rare cases of serious burns have been reported with products of this type

• do not apply to wounds or damaged, broken or irritated skin

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

• a transient burning sensation may occur upon application but generally disappears in several days

• avoid applying into skin folds

Stop use and ask a doctor if

OTC - STOP USE SECTION

• condition worsens

• severe burning sensation, redness, rash or 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

If pregnant or breast-feeding,

OTC - PREGNANCY OR BREAST FEEDING SECTION

ask a health professional before use.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children and pets.

SPL UNCLASSIFIED SECTION

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

adults and children over 12 years:


• apply a thin layer to affected area every 6 to 8 hours
• do not exceed 3 applications in a 24 hour period
• massage into painful area until thoroughly absorbed into skin
AFTER APPLYING, WASH HANDS WITH SOAP AND WAT ER
children 12 years or younger:ask a doctor

Store at no greater than 25°C (77°F).

Inactive ingredients

INACTIVE INGREDIENT SECTION

acrylates/C10-30 alkyl acrylate crosspolymer, alcohol, aminomethylpropanol, C30-45 alkyl cetearyl dimethicone crosspolymer, caprylyl
methicone, ceteth-20 phosphate, cetostearyl alcohol, dicetyl phosphate, dimethicone, edetate disodium, ethylhexylglycerin, glyceryl stearate, hydroxyethyl acrylate/sodium acryloyldimethyl taurate copolymer, isohexadecane, phenoxyethanol, polyoxyl 15
hydroxystearate, polysorbate 60, sorbitan isostearate, steareth-21, tocopherol, water

Questions?

OTC - QUESTIONS SECTION

1-855-446-4345

SPL UNCLASSIFIED SECTION

DIST. BY: PROCTER & GAMBLE, CINCINNATI, OH 45202

NerviveHealth.com

PRINCIPAL DISPLAY PANEL - 2.5 OZ

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NERVIVE™ PAIN RELIEVING LIQUID ROLL-ON

LIDOCAINE HCl & MENTHOL

TARGETS MULTIPLE NERVE PAIN RECEPTORS

MAXIMUM STRENGTH

MEDICATED ROLL-ON NET WT 2.5 OZ (70.9 g)

Nervive Roll-onNervive Roll-on

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
69423-970-032024-07-30C16284748780-11e7a6dab-16d7-a2ce-e063-dadaa90aadf7NERVIVE™ PAIN RELIEVING Liquid Roll-on

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69423-970NERVIVE PAIN RELIEVING LIQUID ROLL-ON (LIDOCAINE HCL AND MENTHOL) LIQUID [THE PROCTER & GAMBLE MANUFACTURING COMPANY]8Legacy NDC20240731_d7c56bf3-80f3-0a67-e053-2995a90abe23.zip

Products#

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

DailyMed product names page 1 of 1 · 25 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
69423-97069423-970-03

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 23 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
1e7957e1-d955-44fd-e063-6294a90a2c79d7c56bf3-80f3-0a67-e053-2995a90abe232024-07-30WarningsExact identifier
spl id: 1e7957e1-d955-44fd-e063-6294a90a2c79
spl set id: d7c56bf3-80f3-0a67-e053-2995a90abe23

Reported adverse events (FAERS/openFDA)#

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