FDA.reportPublic FDA data

NERVIVE™ PAIN RELIEVING CREAM

Manufacturer
The Procter & Gamble Manufacturing Company
Effective date
2026-10-06
Label type
HUMAN OTC DRUG LABEL
Version
6
Source
daily-update
Hydrated at
2026-10-09 01:01:22

Label at a glance#

ProductNervive Pain Relieving Cream
Active ingredientLIDOCAINE HYDROCHLORIDE ANHYDROUS, MENTHOL
Label structure10 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 WATE R children 12 years or younger: ask a doctor

Storage and handling

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%

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.

OVERDOSAGE 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 WATER
children 12 years or younger: ask a doctor

STORAGE AND HANDLING SECTION

Store at no greater than 25°C (77°F).

Inactive ingredients

INACTIVE INGREDIENT SECTION

acrylates/C10-30 alkyl acrylate crosspolymer, alcohol denat., 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

PRINCIPAL DISPLAY PANEL - 3.0 OZ

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NERVIVE™

PAIN RELIEVING CREAM

LIDOCAINE HCl & MENTHOL

PAIN RELIEF CREAM

Blocks

NERVE PAIN SIGNALS

Max Strength Formula^

MEDICATED CREAM NET WT 3.0 OZ (85.1 g)

318318

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130030772042885GTIN-13: 0030772042885
EAN-13: 0030772042885
GTIN-12: 030772042885
UPC-A: 030772042885
GTIN storage (14 digits): 00030772042885		318.jpg
QR code linkQR Codescan.pg.com/01/00030772042885318.jpg
Data codeData Matrix21492499318.jpg

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

Products#

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

DailyMed product names page 1 of 1 · 26 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
84126-31884126-318-03

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 23 matching rows.

Name, UNII, Kind table
NameUNIIKind
LIDOCAINE HYDROCHLORIDE ANHYDROUSEC2CNF7XFPACTIB
MENTHOLL7T10EIP3AACTIB
CARBOMER INTERPOLYMER TYPE B (ALLYL PENTAERYTHRITOL CROSSLINKED)132584PQMOIACT
SORBITAN ISOSTEARATE01S2G2C1E4IACT
POLYSORBATE 60CAL22UVI4MIACT
TOCOPHEROLR0ZB2556P8IACT
C30-45 ALKYL CETEARYL DIMETHICONE CROSSPOLYMER4ZK9VP326RIACT
POLYOXYL 15 HYDROXYSTEARATE71YMM1X75OIACT
CAPRYLYL TRISILOXANEQ95M2P1KJLIACT
EDETATE DISODIUM7FLD91C86KIACT
WATER059QF0KO0RIACT
DIMETHICONE92RU3N3Y1OIACT
DIHEXADECYL PHOSPHATE2V6E5WN99NIACT
AMINOMETHYLPROPANOLLU49E6626QIACT
STEARETH-2153J3F32P58IACT
HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER (45000 MPA.S AT 1%)86FQE96TZ4IACT
ISOHEXADECANE918X1OUF1EIACT
PHENOXYETHANOLHIE492ZZ3TIACT
ETHYLHEXYLGLYCERIN147D247K3PIACT
CETETH-20 PHOSPHATE921FTA1500IACT
GLYCERYL MONOSTEARATE230OU9XXE4IACT
ALCOHOL3K9958V90MIACT
CETOSTEARYL ALCOHOL2DMT128M1SIACT

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
52026-03-24full-release2026-06-01 01:51:15
42025-10-03monthly-update2026-06-03 17:38:28
32024-08-06full-release2026-06-01 00:41:49

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
4dc891c6-4cbe-bad0-e063-6294a90aa3741e8bfb1e-8f5a-d0f3-e063-6294a90a752a2026-03-24WarningsExact identifier
spl set id: 1e8bfb1e-8f5a-d0f3-e063-6294a90a752a

Reported adverse events (FAERS/openFDA)#

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