Storage and handling
Store in a cool, dy place. Do not use if seal is missing or broken.
Viobin, LLC
- Manufacturer
- PHM Brands, LLC | Viobin, LLC
- Effective date
- 2021-07-16
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 1
- Source
- legacy-cache
- Hydrated at
- 2026-08-01 22:39:45
Label at a glance#
ProductViobin, LLC
Active ingredientMENTHOL
Label structure12 sections
Label contents#
Full prescribing information#
OTC - ACTIVE INGREDIENT SECTION
4% Menthol
OTC - PURPOSE SECTION
Topical analgesic
INDICATIONS & USAGE SECTION
For the temporary relief of minor aches and pains of sore muscles and joints associated with backache, arthritis, strains, bruises, sprains
WARNINGS SECTION
For external use only
OTC - WHEN USING SECTION
Avoid contact with eyes or mucous membranes. Do not apply to wounds or damaged skin Do not apply irritated skin or if excesssive irritation develops. Do not bandage or use with a heating pad. Wash hands after use with cool water.
OTC - STOP USE SECTION
If condtiion worsens, or if symptoms persists for more than 7 days or clear up and reoccur.
OTC - KEEP OUT OF REACH OF CHILDREN SECTION
If swallowed, get medical help or contact Poison Control immediately.
OTC - PREGNANCY OR BREAST FEEDING SECTION
Ask a health professional before use.
DOSAGE & ADMINISTRATION SECTION
Apply to affected areas 1 to 2 times daily
STORAGE AND HANDLING SECTION
Store in a cool, dy place. Do not use if seal is missing or broken.
INACTIVE INGREDIENT SECTION
Water, Organic Coconut Oil, Full Spectrum Hemp Extract (Aerial Parts), Emulsyfying Wax (Cetyl Alcohol, Stearyl Alcohol, Polysorbate 60), Stearic Acid, Phenoxyethanol, Xanthan Gum, Tetrasodium Glutamate Diacetate.
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
Products#
Every source-derived product name is available through these pages.
- Viobin, LLC
- Pain Relief Ointment
- STEARIC ACID
- XANTHAN GUM
- MENTHOL
- WATER
- COCONUT OIL
- CETYL ALCOHOL
- STEARYL ALCOHOL
- POLYSORBATE 60
- TETRASODIUM GLUTAMATE DIACETATE
- PHENOXYETHANOL
- CANNABIDIOL
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 78759-005 | 78759-005-03 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| STEARIC ACID | 4ELV7Z65AP | IACT |
| XANTHAN GUM | TTV12P4NEE | IACT |
| MENTHOL | L7T10EIP3A | ACTIB |
| WATER | 059QF0KO0R | IACT |
| COCONUT OIL | Q9L0O73W7L | IACT |
| CETYL ALCOHOL | 936JST6JCN | IACT |
| STEARYL ALCOHOL | 2KR89I4H1Y | IACT |
| POLYSORBATE 60 | CAL22UVI4M | IACT |
| TETRASODIUM GLUTAMATE DIACETATE | 5EHL50I4MY | IACT |
| PHENOXYETHANOL | HIE492ZZ3T | IACT |
| CANNABIDIOL | 19GBJ60SN5 | 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 |
|---|---|---|---|---|---|---|
| d505ded5-c29b-55ca-e053-2a95a90a8c51 | c7444b9e-3020-4049-e053-2995a90a319d | 2022-01-07 | Warnings | c7444b9e-3020-4049-e053-2995a90a319d |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.