Indications and uses
temporarily relieves minor aches and pains of muscle and joints associated with simple backache arthritis strains bruises sprains
Soltice
- Manufacturer
- Oakhurst Company
- Effective date
- 2026-09-24
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 1
- Source
- daily-update
- Hydrated at
- 2026-10-02 01:04:10
Label at a glance#
ProductSoltice
Active ingredientMENTHOL, CAMPHOR (NATURAL)
Label structure13 sections
Dosage and administration
Rub into skin until Soltice is absorbed and disappears Adults and children 2 years of age and over apply to affected area not more than 3 to 4 times daily Children under 2 years of age: ask a doctor
Label contents#
Full prescribing information#
Active Ingredient
Menthol 5.1%
Purpose
Topical Analgesic
Active Ingredient
Camphor 5.1 %
Purpose
Topical Analgesic
Uses
temporarily relieves minor aches and pains of muscle and joints associated with
- simple backache
- arthritis
- strains
- bruises
- sprains
Warnings
For external use only
Do not use
- on irritated skin
- on reddened skin
- on wounds
- on damaged skin.
When using this product
- avoid contact with eyes and mucous membranes (such as the inside of nose or mouth)
- do not bandage tightly.
Stop use and ask doctor if
- condition worsens
- condition does not improve in 7 days
- condition clears up and occurs again within a few days
Keep out of reach of children.
If swallowed, get medical help or contact a Poison Control Center right away
DIRECTIONS:
Rub into skin until Soltice is absorbed and disappears
Adults and children 2 years of age and over
apply to affected area not more than 3 to 4 times daily
Children under 2 years of age: ask a doctor
Inactive Ingredients
eucalyptus oil, glycerin, methyl salicylate, oleic acid, potassium hydroxide, stearic acid, water
Package - Soltice
Products#
Every source-derived product name is available through these pages.
- Soltice
- menthol, camphor
- MENTHOL
- CAMPHOR (NATURAL)
- EUCALYPTUS OIL
- GLYCERIN
- METHYL SALICYLATE
- OLEIC ACID
- POTASSIUM HYDROXIDE
- STEARIC ACID
- WATER
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 45728-100 | 45728-100-01, 45728-100-03 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| MENTHOL | L7T10EIP3A | ACTIB |
| CAMPHOR (NATURAL) | N20HL7Q941 | ACTIB |
| EUCALYPTUS OIL | 2R04ONI662 | IACT |
| GLYCERIN | PDC6A3C0OX | IACT |
| METHYL SALICYLATE | LAV5U5022Y | IACT |
| OLEIC ACID | 2UMI9U37CP | IACT |
| POTASSIUM HYDROXIDE | WZH3C48M4T | IACT |
| STEARIC ACID | 4ELV7Z65AP | IACT |
| WATER | 059QF0KO0R | 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.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.