Exigence One Patch
- Manufacturer
- DirectRx
- Effective date
- 2022-01-10
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 3
- Source
- legacy-cache
- Hydrated at
- 2026-08-01 22:18:44
Label at a glance#
ProductExigence One Patch
Active ingredientMENTHOL, UNSPECIFIED FORM, LIDOCAINE
Label structure13 sections
Contacts and useful links#
Label contents#
Full prescribing information#
OTC - PURPOSE SECTION
Topical Analgesic
WARNINGS SECTION
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
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
If swallowed, get medical help, or contact a Poison Control Central right away.
OTC - PREGNANCY OR BREAST FEEDING SECTION
Ask a health professional before use.
OTC - WHEN USING SECTION
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
Store at 20-25 oC (68-77 oF) and protect from moisture.
INACTIVE INGREDIENT SECTION
polyacrylamide, vinol, sodium polyacrylate; acrylate polymerization, purified water.
OTC - QUESTIONS SECTION
Questions?
(310) 320-0100
OTC - ACTIVE INGREDIENT SECTION
Lidocaine 4%
Menthol 1%
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 72189-296-01 | EA - Each | 72189-296 | ba369579-bbbe-4425-8400-d3222f9d84a0 | 1 | 2022-01-06 |
| 81902-102-01 | EA - Each | 81902-102 | c086303e-c664-465a-9977-af52d8a35d7b | 1 | 2021-09-07 |
Products#
Every source-derived product name is available through these pages.
- Exigence One Patch
- MENTHOL, UNSPECIFIED FORM
- POLYACRYLAMIDE (10000 MW)
- SODIUM POLYACRYLATE (2500000 MW)
- ETHENYL
- LIDOCAINE
- WATER
- ACRYLATES CROSSPOLYMER-6
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 72189-296 | 72189-296-01 |
| 81902-102 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| MENTHOL, UNSPECIFIED FORM | L7T10EIP3A | ACTIB |
| POLYACRYLAMIDE (10000 MW) | E2KR9C9V2I | IACT |
| SODIUM POLYACRYLATE (2500000 MW) | 05I15JNI2J | IACT |
| ETHENYL | PQ2K3G3591 | IACT |
| LIDOCAINE | 98PI200987 | ACTIB |
| WATER | 059QF0KO0R | IACT |
| ACRYLATES CROSSPOLYMER-6 | 4GXD0Q3OS3 | IACT |
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 |
|---|---|---|---|---|---|---|
| 074b730e-ba75-c0de-e063-6294a90a964f | d22c67dd-b8e6-b8bd-e053-2995a90a2041 | 2023-10-09 | Warnings | d22c67dd-b8e6-b8bd-e053-2995a90a2041 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.