Procicept L

Manufacturer
Nocicept Technologies, Inc.
Effective date
2018-01-20
Label type
HUMAN OTC DRUG LABEL
Version
6
Source
legacy-cache
Hydrated at
2026-08-02 01:04:39

Label at a glance#

ProductProcicept L Lidocaine 4%
Active ingredientLIDOCAINE, MENTHOL
Label structure12 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredients                              Purpose

Lidocaine 4%                                         Topical Anesthetic

Menthol 1%                                           Topical Analgesic

OTC - PURPOSE SECTION

Uses

Temporarily relieves minor pain.

WARNINGS SECTION

Warnings

For external use only

OTC - DO NOT USE SECTION

Do not use
On large areas of the body or on cut, irritated or swollen skin
On puncture wounds
For more than one week without consulting a doctor

OTC - WHEN USING SECTION

When using this product

Use only as directed

Read and follow all direction and warnings on this carton

Do not allow contact with eyes

Do not bandage or apply local heat (such as heating pads) to the area of use

OTC - STOP USE SECTION

Stop using and ask a doctor if

Condition worsens

Symptoms persist for more than 7 days or clear up and occur again within a few days

OTC - PREGNANCY OR BREAST FEEDING SECTION

When pregnant or breastfeeding, ask a health professional before use

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

INDICATIONS & USAGE SECTION

Directions

Adults and children over 12 years of age

Apply generously (about the thickness of a nickel) to the affected area as needed, not to exceed 3 applications

DOSAGE & ADMINISTRATION SECTION

Children 12 years and younger

Ask a doctor

INACTIVE INGREDIENT SECTION

Inactive ingredients

benzyl alcohol, soy lecithin, isopropyl palmitate, poloxamer, sorbic acid

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

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Products#

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
70458-10170458-101-02, 70458-101-07

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

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
617acb8f-c519-445a-bc34-c6bf50f910f4896faf91-527d-4de2-a2bb-28169bf957dc2018-01-20WarningsExact identifier
spl id: 617acb8f-c519-445a-bc34-c6bf50f910f4
spl set id: 896faf91-527d-4de2-a2bb-28169bf957dc

Reported adverse events (FAERS/openFDA)#

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