UtaSpray 100 mg/mL
Menthol and Methyl Salicylate · LIQUID · Big 5 Nutrition LLC
No Recall History
Plain English
UtaSpray is a liquid containing menthol and methyl salicylate at 100 mg/mL, taken topical. Manufactured by Big 5 Nutrition LLC.
Key Facts
- Brand Name
- UtaSpray
- Generic Name
- Menthol and Methyl Salicylate
- NDC Code (Product)
82198-0008- Manufacturer
- Big 5 Nutrition LLC
- Strength
- 100 mg/mL
- Dosage Form
- LIQUID
- Route
- TOPICAL
- Marketing Status
- Application #
- M017
- Marketing Start
- 10/01/2022
Recall History
No Recall HistorySide Effects Reported to FDA
FDA FAERS database · These are reported events, not confirmed side effects
amnesia1 reports
anaphylactic reaction1 reports
arthralgia1 reports
aspiration1 reports
asthma1 reports
asthmatic crisis1 reports
bile duct stone1 reports
chills1 reports
cholangitis1 reports
conjunctivitis1 reports
Frequently Asked Questions
What is UtaSpray used for?
UtaSpray contains Menthol and Methyl Salicylate. It is a liquid taken topical. Consult your doctor for specific uses.
Is UtaSpray a controlled substance?
UtaSpray is not classified as a controlled substance by the DEA.
What is the generic name for UtaSpray?
The generic name for UtaSpray is Menthol and Methyl Salicylate. There are 8 other brand versions of Menthol and Methyl Salicylate.
What is the NDC code for UtaSpray 100 mg/mL?
The NDC (National Drug Code) for UtaSpray 100 mg/mL is 82198-0008, listed by Big 5 Nutrition LLC.