Dosage and administration
Adults and children 2 years of age and older: apply to affected area not more than 3 to 4 times daily. Children under 2 years of age, consult a Physician.
Chondro-Pro
- Manufacturer
- MDR Fitness Corp.
- Effective date
- 2019-12-23
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 2
- Source
- full-release
- Hydrated at
- 2026-05-31 23:02:26
Label at a glance#
ProductChondro-Pro Pain Relief Roll On
Active ingredientMENTHOL, UNSPECIFIED FORM
Label structure9 sections
Contacts and useful links#
Label contents#
Full prescribing information#
SPL UNCLASSIFIED SECTION
Drug Facts
Active Ingredients
Menthol 2%
Purpose
Topical analgesic
Indications
for the temporary relief of minor aches and pains of muscles and joints associated with
- arthritis
- simple backache
- strains
- sprains
- bruises
Warnings
- For external use only.
- Avoid contact with the eyes.
- If condition worsens, or if symptoms persist for more than 7 days or clear up and occur again within a few days, discontinue use of this product and consult a Physician.
- Do not apply to wounds or damaged skin.
- Do not bandage tightly.
OTC - KEEP OUT OF REACH OF CHILDREN SECTION
- Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
Directions
- Adults and children 2 years of age and older:
apply to affected area not more than 3 to 4 times daily. - Children under 2 years of age, consult a Physician.
Inactive ingredients
Water, Butylene Glycol, Aloe Barbadensis Leaf Juice, Eucalyptus Globulus Leaf Oil, Methyl Salicylate, Camphor, Mentha Piperita (Peppermint) Oil, Carbomer, Triethanolamine, Propylparaben, Methylparaben, Diazolidinyl Urea, Tetrasodium EDTA.
OTC - QUESTIONS SECTION
Call Us Toll Free:
1 800 MDR-TABS
PRINCIPAL DISPLAY PANEL - 59.1 mL Bottle Label
MDR®
Medical Doctors Research®
Chondro
Pro™
Pain Relief
Roll On
Net wt. 2 fl. oz.
(59.1 mL)
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 68393-349-02 | 2021-01-29 | C162847 | 48780-1 | ba0f9c33-2b2a-a910-e053-dadaa90a0b85 | Chondro-Pro™ Pain Relief Roll On |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 68393-349-02 | Chondro-Pro Pain Relief Roll On | 59.1 mL in 1 BOTTLE, DISPENSING | GEL | 59.1 | 2 |
DailyMed Dashboard NDC Coverage#
Products#
Every source-derived product name is available through these pages.
- Chondro-Pro Pain Relief Roll On
- MENTHOL, UNSPECIFIED FORM
- Camphor (synthetic)
- Water
- Eucalyptus oil
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 68393-349 | 68393-349-02 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| MENTHOL, UNSPECIFIED FORM | L7T10EIP3A | ACTIB |
| Camphor (synthetic) | 5TJD82A1ET | IACT |
| Water | 059QF0KO0R | IACT |
| Eucalyptus oil | 2R04ONI662 | 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 |
|---|---|---|---|---|---|---|
| 639dbf42-6c4b-413c-a24a-110c63c48de3 | a4a42692-5721-425b-9234-0b775b77bbf2 | 2019-12-23 | Warnings | 639dbf42-6c4b-413c-a24a-110c63c48de3 a4a42692-5721-425b-9234-0b775b77bbf2 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.