Centipaine for Pain Control

Manufacturer
Whitestone Products LLC
Effective date
2021-12-23
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 22:21:21

Label at a glance#

ProductCentipaine for Pain Control
Active ingredientLIDOCAINE, MENTHOL, UNSPECIFIED FORM
Label structure14 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredients

Lidocaine 4%

Menthol 1%

OTC - PURPOSE SECTION

Purpose

Topical Analgesic

INDICATIONS & USAGE SECTION

Uses

For the temporary relief of pain.

WARNINGS SECTION

Warnings

For external use only not intended for ingestion.

OTC - DO NOT USE SECTION

Do not use

  • in large quantities, particularly over raw surfaces, or blistered areas.

OTC - WHEN USING SECTION

When using this product

  • Avoid contact with the eyes.

OTC - ASK DOCTOR SECTION

Stop use and ask doctor if

  • condition worsens, or if symtoms persist for more than 7 days or clear up and occur again within a few days.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

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

OTC - PREGNANCY OR BREAST FEEDING SECTION

If pregnant or breast-feeding, ask a health professional before use.

DOSAGE & ADMINISTRATION SECTION

Directions

  • Adults and children 2 years of age and older: Apply to affected area not more than 3 to 4 times a daily.
  • Children under 2 years of age: consult a doctor.

OTHER SAFETY INFORMATION

Other Information

Store at 20-25 oC (68-77 oF) and protect from moisture.

INACTIVE INGREDIENT SECTION

Inactive ingredients

polyacrylamide, vinol, sodium polyacrylate; acrylate polymerization, purified water.

OTC - QUESTIONS SECTION

Questions?

(310) 320-0100

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

boxbox

Products#

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DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
81902-12081902-120-03

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
06f133b3-b5d0-1850-e063-6394a90a9ff4dfabe851-3c58-4161-b3d4-ef93748052bb2023-10-05WarningsExact identifier
spl set id: dfabe851-3c58-4161-b3d4-ef93748052bb

Reported adverse events (FAERS/openFDA)#

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