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#
Contacts and useful links#
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
Products#
Every source-derived product name is available through these pages.
- Centipaine for Pain Control
- Lidocaine 4%, Menthol 1%
- POLYACRYLAMIDE (10000 MW)
- ETHENYL
- ACRYLATES CROSSPOLYMER-6
- SODIUM POLYACRYLATE (2500000 MW)
- WATER
- LIDOCAINE
- MENTHOL, UNSPECIFIED FORM
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 81902-120 | 81902-120-03 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| POLYACRYLAMIDE (10000 MW) | E2KR9C9V2I | IACT |
| ETHENYL | PQ2K3G3591 | IACT |
| ACRYLATES CROSSPOLYMER-6 | 4GXD0Q3OS3 | IACT |
| SODIUM POLYACRYLATE (2500000 MW) | 05I15JNI2J | IACT |
| WATER | 059QF0KO0R | IACT |
| LIDOCAINE | 98PI200987 | ACTIB |
| MENTHOL, UNSPECIFIED FORM | L7T10EIP3A | ACTIB |
Source Document#
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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| 06f133b3-b5d0-1850-e063-6394a90a9ff4 | dfabe851-3c58-4161-b3d4-ef93748052bb | 2023-10-05 | Warnings | dfabe851-3c58-4161-b3d4-ef93748052bb |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
