NERVIVE™ PAIN RELIEVING SPRAY

Manufacturer
The Procter & Gamble Manufacturing Company
Effective date
2026-10-05
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
daily-update
Hydrated at
2026-10-07 01:02:06

Label at a glance#

ProductNervive Pain Relieving
Active ingredientLIDOCAINE HYDROCHLORIDE, MENTHOL
Label structure16 sections

Dosage and administration

adults and children over 12 years of age and older: spray the affected area not more than 3 to 4 times daily product will dry quickly on its own, and does not need to be rubbed in wash hands thoroughly with soap and water after each use children under 12 years of age: 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 fire, sparks, and heated surfaces. Contents under pressure, do not puncture or incinerate container. Exposure to temperatures above 120°F may cause bursting.

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 label.
  • avoid contact with eyes and mucous membranes.
  • do not spray in face or mouth
  • rare cases of serious burns have been reported with products of this type
  • do not apply to wounds or damaged, broken, blistered 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 of age and older:

  • spray the affected area not more than 3 to 4 times daily
  • product will dry quickly on its own, and does not need to be rubbed in
  • wash hands thoroughly with soap and water after each use

children under 12 years of age: ask a doctor

Store at no greater than 25°C (77°F).

Inactive ingredients

INACTIVE INGREDIENT SECTION

alcohol denat., isopropyl myristate, propylene glycol, water

Questions?

OTC - QUESTIONS SECTION

1-855-446-4345

SPL UNCLASSIFIED SECTION

Grip cap. Squeeze lines firmly.

Pull up & twist.

SPL UNCLASSIFIED SECTION

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

PRINCIPAL DISPLAY PANEL - 4.5 OZ

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NERVIVE™

PAIN RELIEVING SPRAY

LIDOCAINE HCl & MENTHOL

PAIN RELIEF SPRAY

Blocks NERVE PAIN SIGNALS

Starts Working in Minutes at the Source

Great for Hard to Reach Areas like Legs & Feet

NET WT 4.5 OZ (127.6 g)

319319

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130030772171967GTIN-13: 0030772171967
EAN-13: 0030772171967
GTIN-12: 030772171967
UPC-A: 030772171967
GTIN storage (14 digits): 00030772171967
319.jpg
QR code linkQR Codescan.pg.com/01/00030772171967319.jpg
Data codeData Matrix21483059319.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
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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 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
84126-31984126-319-45, 84126-319-05

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
22026-03-24full-release2026-06-01 01:51:17

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
Nervive Pain RelievingLIDOCAINE HCL AND MENTHOLThe Procter & Gamble Manufacturing Company32f8d0f3-d18d-1a45-e063-6294a90a6ad32026-03-24WarningsExact identifier
ndc (package): 84126-319-45
ndc (package): 84126-319-05
ndc (product): 84126-319
ndc11 (package): 84126031905
ndc11 (package): 84126031945
spl set id: 32f8d0f3-d18d-1a45-e063-6294a90a6ad3

Reported adverse events (FAERS/openFDA)#

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