Indications and uses
temporarily relieves the minor aches and pains of muscles and joints associated with: simple backaches arthritis strains bruises sprains
OLP PAIN-X
- Manufacturer
- ohio lab pharma
- Effective date
- 2018-11-26
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 13
- Source
- legacy-cache
- Hydrated at
- 2026-08-02 00:45:34
Label at a glance#
ProductOLP PAIN-X
Active ingredientMENTHOL, UNSPECIFIED FORM
Label structure12 sections
Dosage and administration
adults and children 12 years of age and older: apply to affected area not more than 3 to 4 times daily children under 12 years of age: ask a doctor
Contacts and useful links#
Websitewww.ohiolabpharma.us
www.ohiolabpharma.us
www.ohiolabpharma.usLabel contents#
Full prescribing information#
Active ingredient
Menthol 2.5%
Purpose
Topical analgesic
Uses
temporarily relieves the minor aches and pains of muscles and joints associated with:
- simple backaches
- arthritis
- strains
- bruises
- sprains
Warnings
for external use only
Do not use
- on wounds or damaged skin
- with a heating pad
- on a child under 12 years of age with arthritis-like conditions
When using this product
- avoid contact with eyes or mucous membranes
- do not bandage tightly
Stop use and ask a doctor if
- condition worsens or symptoms persist for more than 7 days
- symptoms clear up and occur again within a few days
- excessive skin irritation occurs
Directions
- adults and children 12 years of age and older: apply to affected area not more than 3 to 4 times daily
- children under 12 years of age: ask a doctor
Other information
- store at 20° to 25°C (68° to 77°F)
Inactive ingredients
Vitamin E, Propylene glycol,Polysorbate 80,Water, Isopropyl alcohol,Carbomer interpolymer typ A, edta, Methylparaben, Propylparaben.
Questions?
Principal display panel 42.5 g tube carton
VANISHING SCENT
OLP PAIN-X
MENTHOL PAIN RELIEVING GEL
work on all types of minor arthritis pain
POWERFUL PAIN RELIEF FROM MINOR ARTHRITIS, BACKACHE, MUSCLE AND JOINT PAIN
NET WT. 1.5 OZ (42.5 g)
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 70648-005-01 | 2020-08-24 | C162847 | 48780-1 | 9d75b9cf-f8d5-f424-e053-dadaa90a57ce | 3a637b9b-3f9d-2c3c-e054-00144ff8d46c |
| 70648-005-01 | 2020-01-31 | C162847 | 48780-1 | 9d75b9cf-f8d5-f424-e053-dadaa90a57ce | 3a637b9b-3f9d-2c3c-e054-00144ff8d46c |
Products#
Every source-derived product name is available through these pages.
- OLP PAIN-X
- MENTHOL
- CARBOMER INTERPOLYMER TYPE A (55000 CPS)
- METHYLPARABEN
- PROPYLPARABEN
- .ALPHA.-TOCOPHEROL
- EDETATE DISODIUM
- MENTHOL, UNSPECIFIED FORM
- POLYSORBATE 80
- ISOPROPYL ALCOHOL
- WATER
- PROPYLENE GLYCOL
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 70648-005 | 70648-005-01 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| CARBOMER INTERPOLYMER TYPE A (55000 CPS) | 59TL3WG5CO | IACT |
| METHYLPARABEN | A2I8C7HI9T | IACT |
| PROPYLPARABEN | Z8IX2SC1OH | IACT |
| .ALPHA.-TOCOPHEROL | H4N855PNZ1 | IACT |
| EDETATE DISODIUM | 7FLD91C86K | IACT |
| MENTHOL, UNSPECIFIED FORM | L7T10EIP3A | ACTIB |
| POLYSORBATE 80 | 6OZP39ZG8H | IACT |
| ISOPROPYL ALCOHOL | ND2M416302 | IACT |
| WATER | 059QF0KO0R | IACT |
| PROPYLENE GLYCOL | 6DC9Q167V3 | 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 |
|---|---|---|---|---|---|---|
| ada3e4d6-e25b-6278-e053-2a95a90a03da | 3a637b9b-3f9d-2c3c-e054-00144ff8d46c | 2020-08-24 | Warnings | 3a637b9b-3f9d-2c3c-e054-00144ff8d46c |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.