Drugplain

AleveX 5.5 mg/g

camphor and menthol · SPRAY · Bayer HealthCare LLC

No Recall History
Plain English

AleveX is a spray containing camphor and menthol at 5.5 mg/g, taken topical. Manufactured by Bayer HealthCare LLC.

Key Facts

Brand Name
AleveX
Generic Name
camphor and menthol
NDC Code (Product)
0280-0049
Manufacturer
Bayer HealthCare LLC
Strength
5.5 mg/g
Dosage Form
SPRAY
Route
TOPICAL
Marketing Status
Application #
M017
Marketing Start
04/01/2021

Recall History

No Recall History

Side Effects Reported to FDA

FDA FAERS database · These are reported events, not confirmed side effects

drug ineffective8 reports
choking4 reports
dyspnoea4 reports
abdominal discomfort3 reports
application site pain3 reports
nausea3 reports
application site pruritus2 reports
dyspepsia2 reports
haemorrhage2 reports
hypoaesthesia2 reports

Full Prescribing Information

Source: FDA Drug Label (SPL)For healthcare professionals

Indications & Usage

For the temporary relief of minor aches and pains of muscles and joints associated with: arthritis simple backache strains sprains bruises Provides penetrating pain relief

Dosage & Administration

Directions Adults and children 12 years of age and older Shake well before use Apply to affected area not more than 3 to 4 times daily Do not apply to face Use in a well-ventilated area and avoid inhalation Wash hands with soap and water after use if product comes in contact with hands Children under 12 years of age Ask a doctor

Warnings

Warnings For external use only Flammable : do not use near heat, flame, or while smoking. Do not use if you have ever had an allergic reaction to this product or any of its ingredients When using this product avoid contact with the eyes and mucous membranes use only as directed. Intentional misuse by deliberately concentrating and inhaling the contents can be harmful or fatal contents under pressure. Do not puncture or incinerate. Do not store at temperature above 120ºF do not bandage tightly do not use with a heating pad, medicated patch or other types of local heat do not apply to wounds or damaged, broken or irritated skin Stop use and ask a doctor if condition worsens or irritation develops pain, swelling or blistering develops where product was applied redness or severe burning develops where product was applied symptoms persist for more than 7 days or clear up and occur again within a few days If pregnant or breast-feeding, ask a health professional before use. If swallowed, get medical help or contact a Poison Control Center right away.

Frequently Asked Questions

What is AleveX used for?

AleveX contains camphor and menthol. It is a spray taken topical. Consult your doctor for specific uses.

Is AleveX a controlled substance?

AleveX is not classified as a controlled substance by the DEA.

What is the generic name for AleveX?

The generic name for AleveX is camphor and menthol. There are 10 other brand versions of camphor and menthol.

What is the NDC code for AleveX 5.5 mg/g?

The NDC (National Drug Code) for AleveX 5.5 mg/g is 0280-0049, listed by Bayer HealthCare LLC.

Product NDC

0280-0049

Package NDC

0280-0049-01

Other AleveX Dosages

Other Camphor Brands

See all →

Not medical advice. Always consult your doctor or pharmacist before making any medication decisions.

Data from openFDA · Public domain (CC0 1.0)